Clinical Research Positions
Clinical research trials require a variety of people working together to execute a proper trial. There are several different career paths in clinical research, from technical positions to administrative positions.
Clinical Research Associate (CRA), Field Monitor, Clinical Monitor or Trial Monitor
The clinical research associate supervisors and monitors are requested and paid by sponsors who hire them to help with the administrative parts of clinical trials. Their duties include the filing of data, reviewing of case reports, performing investigational product accountability, and making sure that all necessary items are properly filed and documented. They also assist with pharmaceutical research, devices research, and biologics research. They ensure that good clinical practices are followed and that protocols are observed. For those interested in becoming a Clinical Research Associate, detailed training can be found here.
Clinical Research Data Manager
Clinical research data managers are in charge of the systems that produce data. Data managers review the protocol for trials before they start. They go through all the data involved in clinical trials strategically and analytically. They also review regulations, prepare protocols, and help the senior manager to ensure that the clinical trials are carried on smoothly. They are in charge of the monitoring, documentation, and information of all research studies. Learn how to manage clinical research data with our Clinical Trials Assistant Training.
Clinical Research Scientist
The clinical research scientist conducts clinical research trial roles that require years of working on clinical trials and clinical trial sites. They conduct a scientific test and ensure that there is proper monitoring of clinical research. They are also familiar with submission processes of clinical research studies, drawing up regulation affairs frameworks, assessment of study, and so on. To dive deeper into this role, consider our Advanced Clinical Research Project Manager Certification.
Biostatistician
The biostatistician operate when there is a compilation of clinical research data. The biostatistician sets up parameters for data collection clinical research products use to fulfill certain criteria. They also analyze all the clinical trial data and come up with a documented report that contains the results. Enhance your skills in biostatistics with our Medical Monitor Certification.
These clinical research positions above are regarded as some of the highest and high paying clinical research professionals positions in the world right now.
What are you waiting for? Register for courses get certified and start practicing.
Take courses from CCRPS and learn more on how to become a clinical research professional.
Discover more from Clinical Research Training | Certified Clinical Research Professionals Course.
Clinical Research Courses for CTA and CRA
Clinical research courses are necessary to ensure that there are enough competent, responsible, and efficient clinical research professionals in the clinical research field. In this article, we'll be paying attention to the clinical research courses for Clinical Trial Assistants (CTAs), and Junior or Senior Clinical Research Associates (CRAs).
CTA
CTAs are one of the crucial role players in the clinical research process. They maintain the project's records, files, documentation and store them. They also assist with the review of clinical project records for accuracy and make them complete and ready for audit.
The CTA course offered at CCRPS are for those who are new to the job and want to cover the basics and principles of clinical research.
The program will highlight ICH GCP as the clinical research basis to introduce the new CTAs to drug development and to be familiar with the rules. It covers clinical studies operations, data management, and informatics, investigational product development and regulation, etc.
CRA
Junior Clinical Research Associates (CRAs) are introduced to Clinical Research, the life cycle of a clinical trial, how to monitor the clinical trial activities at different stages, clinical data monitoring, and management. It helps student become more familiar with the job of a CRA from the start of a clinical trial to its end. The course offered are similar to as those of a CTA’s.
Senior Clinical Research Associates (CRAs) are given opportunities to face more complex clinical trials and site management issues. The program will highlight the importance of international research as well as the role of the ICH GCP process. It also gives updates on the overview of current legislative requirements including:
guidance on substantial trial modifications,
improving the recruitment process of subjects and site staff
how to prioritize and upgrade clinical trial monitoring tasks and activities
accurate monitoring and reporting, dealings with non-compliance
efficient tracking and coaching and mentoring junior CRAs
The courses offered will expand the knowledge and improve the monitoring skills to help take and make the right actions and decisions to resolve site issues.
Each of the courses is designed to produce competent clinical research professionals.
Take courses from CCRPS and learn more on how to become Clinical Trial Assistants, and Junior and Senior Clinical Research Associates.
Take courses from CCRPS and learn more on how to become a clinical research professional.
Here are some courses you might consider:
Clinical Research Coordinator Certification - Ideal for those looking to coordinate clinical trial activities.
Pharmacovigilance Certification - Focuses on drug safety and adverse effects management.
CRA Certification - Prepares you for the role of Clinical Research Associate.
ICH-GCP Certification - Essential for professionals needing to understand Good Clinical Practice guidelines.
Clinical Trials Assistant Training - Provides foundational knowledge for those starting in clinical trials.
Advanced Clinical Research Project Manager Certification - For experienced professionals aiming for project management roles.
Advanced Principal Investigator Physician Certification - Tailored for physicians leading clinical trials.
Medical Monitor Certification - Designed for those overseeing the medical aspects of clinical trials.
Discover more from Clinical Research Training | Certified Clinical Research Professionals Course
Online Clinical Research Assoicate (CRA) Training
Clinical research associate training is the grooming of clinical researchers to become associates. It's a promising career in the clinical research industry. Any worth-while training will include everything you need to know to about the job and become one of the best.
Clinical Research Associates are those responsible for the planning, setting up, and coordinating clinical trials. They provide technical assistance for experiments, make sure that the scientists that are involved in the clinical research trials comply with regulatory standards, and also collect results during the clinical trials. When the trials are over they are also to be involved in the presentation of the results to the public in a manner that is useful and understandable. Enhance your skills as a Clinical Research Associate with CRA training.
The amazing part about being a clinical research associate is that jobs are available in both the laboratory and office setting.
To be an associate in clinical research you need a minimum degree of a bachelor's or master's degree in the clinical research field of study or a related field. They have the key responsibilities of designing and implementing clinical research trials, to train staff, to monitor progress, to screen test subjects, to present findings, and to help maintain the database of all clinical research trainees.
The median salary of a clinical research associate boasts of $61,932 annually. It is one of the most attractive salaries for someone with a science degree, as it is always on a rise and there is always a ready market for clinical research professionals.
A clinical trial is a method in which new medical treatments and pharmaceuticals are developed and experimented and this is where clinical research associates come in. They are an integral part of the process, as they work with teams to design, implement, and organize research trials to test out the effectiveness of the proposed medicines on humans. They are responsible for the different parts of clinical trials which include, training of staff, screening test subjects, monitoring the progress of staff, present findings, and maintain the database. Communication skills, science knowledge, and a strong mathematics knowledge base are the core skills you need in the clinical research profession. For those interested in more specialized roles, consider the Advanced Clinical Research Project Manager Certification or the Advanced Principal Investigator Physician Certification.
You can come from a variety of medical sciences or health-related fields, such as a nursing background as an RN. Courses offered expand on clinical related ethics, team management, and research methodologies.
CRA training certificate examination comes with one of the three combinations of education and experience.
High school diploma and 6,000 hours of experience.
An associate degree in clinical research fields and 4,500 hours of experience, or
A Bachelor's, Master's, or Registered Nurse degree and 3,000 hours of clinical research experience.
Get a clinical research associate certificate from certified clinical research professionals course, and earn your way to one of the most lucrative fields in clinical research. At CCRPS, we support online learning, so you can take the classroom everywhere. Learn more about Clinical Research Coordinator training and Pharmacovigilance Certification to broaden your expertise.
Take courses from CCRPS and learn more on how to become a clinical research professional. Further your understanding of good clinical practices with the ICH-GCP course.
Discover more from Clinical Research Training | Certified Clinical Research Professionals Course
CRA Exam Questions
29.Allocable costA cost that can be assigned to a project or an activity based on the relative benefits received30.allowable only if approved by the sponsoring agencyAccording to OMB Circular A-21, costs incurred prior to the project start date are:31.All vertebrate animalsThe Federal Animal Welfare Act applies to which of the following animal species32.AnnuallyIf an institution of higher education is subject to OMB Circular A-133, when must it have an independent audit?33.The Anti-Kickback Act of 1986Which of the following aims at deterring subcontractors from making payments and contractors from accepting payments for the purpose of improperly obtaining or rewarding favorable treatment in connection with a prime contract or a subcontract relating to a prime contract?34.An anti-lobbying certification is required on federal grants, cooperative agreements and contracts exceeding a MINIMUM of:
a. $100,000
b. $500,000
c. $1,000,000
d. 10,000,000a. $100,00035.approval of student's embassyIn order for a foreign national doctoral student researcher to work on a federal grant in an American institution, it is necessary for the student to have36.Assure that the highest quality proposals are selected for funding in an equitable mannerWhich of the following is the primary purpose of federal proposal review processes?37.An award similar to a grant, and anticipates having substantial involvement in research activities once the award has been made.What is cooperative agreement?38.Award terms and conditionsA Notice of Award typically includes which of the following
39.Basic and containment procedures designed to protect personnel and the environmentWhich of the following best describes essential laboratory biosafety levels in medical research?40.Bayh-Dole ActWhich of the following was enacted as a uniform patent policy among the many federal agencies that fund research?41.BequestsA type of donation or gift with few or no conditions specified. Gifts may be provided to establish an endowment or to provide direct support for existing programs.42.Break refreshments at a project sponsored workshopUsing the criteria contained in 2 CFR 220, OMB Circular A-21, which of the following costs would most likely be allowable as a direct expenditure item on a federal grant?43.Budget period is yearly. Project period is the life of the contract.What's the difference between budget period and project period?44.a cabinet-level departmentThe Office for Human Research Protection is administered by45.A career development programAn employee in a position which does not enable realization of full potential would benefit most from46.cash flow statementAn important tool you may use to measure and track the flow of
cash into and out of your operation47.Certifications and representationsJust-In-Time initiatives postpone the submission of which of the following items until a decision to make an award is reached?48.Change in allocation within a single budget categoryWhich of the following changes does not require prior National Science Foundation approval?49.Change OrderA written order signed by the contracting officer, directing the contractor to make changes that the changes clause of the contract authorizes the contracting officer to order without the consent of the contractor.50.Chief Executive Officer or Vice President of ResearchWho appoints the chair for each committees at universities
$40,000If an agency requires 20% cost sharing of the total project for a particular program and a proposal is requesting $200,000 from agency, what is the additional amount that the institution must cost share?2.$50,000An investigator on a NIH grant has permission to rebudget $50,000 in supply monies into equipment. If the Institution's facilities and administrative cost (indirect cost) rate (based on MTDC) is 50% how much money will be available for the equipment3.$100,000An anti-lobbying certification is required on federal grants, cooperative agreements, and contracts exceeding a MINIMUM of4.$165,000An institution has an indirect cost rate of 40%. A research project is budgeted at $125,000 in direct costs including an item of equipment at $25,000 which is the only item excluded from the indirect cost base. What is the total cost for the project?5.1.Publicly known information.2. Already known information.3. Information received from others. 4. Information shared with others. 5. Independently developed information. 6. Information not included in the nondisclosure agreement.What is not included in a Nondisclosure Agreement?6.1) Resubmit 2)Appeal 3)Advice to look for other opportunitiesWhat happens to a proposal if it isn't funded?7.2NIH limits how many resubmissions on proposals?8.2 CFR 215 OMB A-110Administration Regulation for Education Institutes, Hospitals, and Non profits9.2 CFR 220, OMB Circular A-21Deals with cost determination but does not identify the circumstance or dictate the participation in the financing of a project
10.2 CFR 225 OMB A-87Cost Principles for State, Local, and Indian Tribal11.2 CRF 215 (OMB Circular A-110) provides regulations governing which of the following for educational institutions?
a. Administrative requirements for contracts
b. Administrative requirements for grants and cooperate agreements
c. Cost principles for grants and cooperative agreements only
d. Administrative requirements and cost principles for grants and cooperative agreementsb. Administrative requirements for grants and cooperate agreements12.3 years from submission of final report of expendituresRecipients of federal grant funds must retain records for a MINIMUM of13.5 membersAn IRB is required to have at least:14.6-9 monthsThe National Science Foundation indicates decisions on the funding of grant proposals should normally take15.26%The administrative cap on federal negotiated F&A rates is equal to16.90Under Expanded Authority, pre-award costs up to _____ days prior to the effective date of the award the PI can accrue charges before the award start date.17.90 daysIf final financial reporting (FS 425 Report) to federal agencies is not completed with in the typical ___ days, the institution is out of compliance18.90 daysWhen granted expanded authorities, pre-award costs on a federal grant may be incurred by an institution within a MAXIMUM of how many days prior to the official start date?19.90 daysHow many days do recipients of federal grants funds have to submits final reports after completion of the project?
20.A-102State and local governments are subject to which of the following OMB Circulars?21.AbstractShould be 5,000 to 25,000 words in length. This summary should demonstrate to the reader the most important parts of each of the sections of the research proposal in around 200 words.22.Accept, Decline or NegotiateWhen an award is made an institution has the following options.23.Access to federally funded research data is required under the:
a. Solomon Act
b. Davis-Bacon Act
c. Shelby Amendment
d. Stevens Amendmentc. Shelby Amendment24.According to federal regulations, which of the following must be included in an Institution Review Board?
a. Ethicist
b. Attorney
c. Member of the clergy
d. Member unaffiliated with the institutiond. Member unaffiliated with the institution25.Acquisition of property or servicesA procurement contract is used for the purpose of26.Administrative requirements for grants and cooperative agreements only2 CFR 215, OMB Circular A-110 provides regulations governing which of the following for educational institutions?27.AdobeWhat is required to use Grants.gov28.advise student to apply to the federal agency to request a proposal 90 days after proposal was submittedIf a graduate student comes into a university sponsored research office claiming that because of the federal Freedom of Information Act (FOIA) he has the right to obtain a copy of a recently submitted proposal, the research administrator should
29.Allocable costA cost that can be assigned to a project or an activity based on the relative benefits received30.allowable only if approved by the sponsoring agencyAccording to OMB Circular A-21, costs incurred prior to the project start date are:31.All vertebrate animalsThe Federal Animal Welfare Act applies to which of the following animal species32.AnnuallyIf an institution of higher education is subject to OMB Circular A-133, when must it have an independent audit?33.The Anti-Kickback Act of 1986Which of the following aims at deterring subcontractors from making payments and contractors from accepting payments for the purpose of improperly obtaining or rewarding favorable treatment in connection with a prime contract or a subcontract relating to a prime contract?34.An anti-lobbying certification is required on federal grants, cooperative agreements and contracts exceeding a MINIMUM of:
a. $100,000
b. $500,000
c. $1,000,000
d. 10,000,000a. $100,00035.approval of student's embassyIn order for a foreign national doctoral student researcher to work on a federal grant in an American institution, it is necessary for the student to have36.Assure that the highest quality proposals are selected for funding in an equitable mannerWhich of the following is the primary purpose of federal proposal review processes?37.An award similar to a grant, and anticipates having substantial involvement in research activities once the award has been made.What is cooperative agreement?38.Award terms and conditionsA Notice of Award typically includes which of the following
39.Basic and containment procedures designed to protect personnel and the environmentWhich of the following best describes essential laboratory biosafety levels in medical research?40.Bayh-Dole ActWhich of the following was enacted as a uniform patent policy among the many federal agencies that fund research?41.BequestsA type of donation or gift with few or no conditions specified. Gifts may be provided to establish an endowment or to provide direct support for existing programs.42.Break refreshments at a project sponsored workshopUsing the criteria contained in 2 CFR 220, OMB Circular A-21, which of the following costs would most likely be allowable as a direct expenditure item on a federal grant?43.Budget period is yearly. Project period is the life of the contract.What's the difference between budget period and project period?44.a cabinet-level departmentThe Office for Human Research Protection is administered by45.A career development programAn employee in a position which does not enable realization of full potential would benefit most from46.cash flow statementAn important tool you may use to measure and track the flow of
cash into and out of your operation47.Certifications and representationsJust-In-Time initiatives postpone the submission of which of the following items until a decision to make an award is reached?48.Change in allocation within a single budget categoryWhich of the following changes does not require prior National Science Foundation approval?49.Change OrderA written order signed by the contracting officer, directing the contractor to make changes that the changes clause of the contract authorizes the contracting officer to order without the consent of the contractor.50.Chief Executive Officer or Vice President of ResearchWho appoints the chair for each committees at universities
51.A citation of the contract clause authorizing the terminationWhich of the following information must be included in the notification by a federal officer to the contractor to terminate a contract for convenience52.Clinical trial AgreementWhich of the Following types of documents is most appropriate for testing the efficacy and safety of a new drug, device, or vaccine?53.Code of Federal RegulationsThe following provides information on patent rights and responsibilities currently applicable to universities and federally sponsored projects54.cognizant agencyA Federal agency responsible for negotiating and approving facilities and administrative cost rate for an education institution on behalf of all other federal agencies is referred to as the55.Commons Business DailyWhich of the following sources is not commonly used for federal funding opportunities?56.Compliance approvalsRetention of which records are required by the OMB57.Contact legal, then contact program officer over concernsIf a PI received an award and his wife is using the lab and charging to the award. How would you handle it?58.The contractor fails to perform the services within the time specified or any extensionWhich of the following is a reason for a federal contracting officer to send a "Show Cause" notice to a contractor?59.Contract Work Hours and Safety Standards ActThis act would require that certain contracts contain a clause specifying that no laborer or mechanic doing any part of the work contemplated by the contract would be required or permitted to work more than a certain number of hours in any workweek60.control commodities and is governed by Department of CommerceIn Export Control, what does Export Administration Regulation control and who governs it61.control money: Governed by Department of Treasury.In Export Control, what does Office of Foreign Assets Control control and who governs it
62.Cooperative Research And Technology Enhancement Act hopes to enhance research among Universities, private and public sectors, by treating joint inventions as if they are a single owner but only if the collaborators sign an agreement prior to the invention being created.What is the CREATE Act?63.CopyrightIn which of the following areas of intellectual property is the concept of work-for-hire germane64.Cost Accounting StandardsIt is the ___________ that dictate the way in which a contractor must maintain its accounting system.65.Cost Accounting Standards (CAS) must be applied to awards:
a. without federal funding
b. received from any funding source
c. for federal contracts over $500,000
c. for all federal awards covered by 2 CFR 230 (OMB Circular A-122)c. for federal contracts over $500,00066.Cost of Living Allowance COLAgranted to employees based in a foreign city, where cost of living is higher than in Washington, D.C.67.Cost Principals for Educational InstitutesWho is the 2 CRF 220, OMB Circular A-21 for68.A cost reimbursement sub agreementRequires that the subrecipient use best efforts to complete the research
69.Cost sharing must be:
a. verifiable from records
b. included with other federal awards
c. paid from federal funds if it is a fellowship
d. donated third party contributionsa. verifiable from records70.cost sharing occurs when the sponsored program requires financial support for the project from the awarded institution as a condition of the award.What is involuntary committed (mandatory) cost sharing?71.Data Management Plan RequirementNo more than 2 pages and must describe how the proposal will conform to NSF policy on dissemination and sharing of research results.72.Data sharing plan/ Publish and ShareApplicant who are planning to share data may wish to describe briefly the expected scheduled for data sharing, the format of the final data set, the documentation to be provided, whether or not any analytic tools also will be provided and so on ...73.Debarment and suspension rulesWhich of the following is included in 2 CFR 215, OMB Circular A-110?74.Default and convenienceTwo critical termination clauses of the General Provisions of a federal contract75.Department of AgricultureWhich agencies is responsible for administering the Animal Welfare Act?76.Department of EnergyWhich of the following agencies does NOT fund health science research77.Director of Human ResourceWho should administer progressive discipline to an employee?78.the Director of the institution's animal careAs required an IACUC Committee must contain all but one of the following a. a Doctor or Veterinary Medicine, b. a practicing scientist experienced in research with animals, c. the Director of the institution's animal care facility, d. a person not affiliated with the institution79.Each calendar yearOMB Circular A-21, time and effort reporting must be submitted to the institution a MINIMUM of once
80.Each organization using animals in Public Health Service projects must provide written assurance of its compliance with:
a. regulations requiring full-time staff veterinarian
b. provisions for an organizational program for the care and use of animals
c. standard for accreditation with the American Association for Accreditation of Laboratory Animal Care
d. requirements for organizational training and instruction program in the human practices of animal care and used. requirements for organizational training and d. requirements for organizational training and instruction program in the human practices of animal care and use81.Efficient and effective operations and reliable financial reporting are the objectives of:
a. internal controls
b. research compliance
c. cost transfer processes
d. postaward administrationa. internal controls82.electronic funds transferThe federal government prefers to disburse funds under federal grants via83.enacted to assure that a fair portion of federal contracts are placed with small businesses.What is the Small Business Act?84.Equipment donated at fair market valueIs allowable as cost sharing85.Established fundamental national policy for the environment and established the council on environmental qualityWhat is the National Environmental Policy Act?86.Evaluation PlanIt is important to define carefully and exactly how success will be determined.
87.E-VerifyFAR 52.222-54, which requires that federal contractors or subcontractor verify the employment eligibility of all new hires on a contract through an electronic screening database.88.Every 3 yearsHow often do approved animal protocols need to be reviewed by the Institutional Animal Care and Use Committee (IACUC)89.Executive Branchbranch of the government is responsible for enforcing the laws of the land. The president, vice president, department heads (cabinet members), and heads of independent agencies carry out this mission.90.Executive Level II $181,500NIH Salary cap is at what percentage?91.Executive Level I, II, IIIWhat is the highest level of salary?92.Executive Orders 8248 and 11541Establishing the divisions of the Executive Office of the President and defining their functions and duties
Source and -Prescribing the duties of the Office of Management and Budget and the Domestic Council in the Executive Office of the President93.Expanded AuthoritiesDelegates to grantees authorization of one year, no cost extension94.Expanded Authority_____waives certain prior approval requirements by a federal sponsoring agency. It is used only for changes that are necessary for the completion of the project within its original scope and original total budget.95.FabricationMaking up data or results and recording or reporting them96.A facilities & administrative costs (indirect cots) rate is usually established based on:
a. prior actual costs
b. reimbursed costs
c. capital expenses
d. unaudited expensesa. prior actual costs
97.A facilities and administrative cost (indirect cost) may be a direct cost if:
a. it meets the definition of allocable
b. "unlike circumstances" are present
c. normally allowable on federal or federal flow-through awards
d. the award activities are like those generally charged as facilities and administrative costs (indirect costs)b. "unlike circumstances are present98.Faculty have share in the companyConflict of interest may exist when medical faculty members conduct drug clinical tests for a company if99.A faculty member has a 5-yar federal NIH grant which will terminate 8/31, with $14,000 remaining on 7/15 of the same year. A competing continuation was recommended for approval but not funded. Which of the following is the most appropriate advise for the research administrator to give to the member
a. buy as much equipment as possible before the grant year ends
b. request a second review of the continuation application for the NIH
c. transfer laboratory personnel salaries to the to use up the remaining funds
d. request a 1-year, no-cost extension of the grant while revised continuation is under preparationd. request a 1-year, no-cost extension of the grant while revised continuation is under preparation100.F&A is not allowed to be charged on the following?Participant support*, equipment, capital equipment, patient care, tuition, building renovations, rental costs for non-University owned space, scholarships/fellowships, Subawards in excess of $25,000.
*NSF only
101.FalsificationManipulating research materials, equipment, or processes, or changing or omitting data or results such that the research is not accurately represented in the research record102.FARIn order for a contractor to be awarded a federal contract, he must comply with the provisions set forth by:103.FARThe overall guiding principle of __________ is to have an acquisition system that can satisfy customer's needs yet minimize administrative overhead without sacrificing integrity, fairness, openness and public policy objectives.104.A federal agency responsible for negotiating and approving facilities and administrative cost (indirect costs) rates for an educational on behalf of all other federal agencies in referred to as the:
a. lead agency
b. cognizant agency
c. sponsoring agency
d. governmental agencyb. cognizant agency105.Federal commonsWhat is an Internet grants management portal which serves the grantee organization community?106.Federal expanded authorities permit which of the following without additional sponsor approvals?
a. Rebudgeting
b. Change of the Institution
c. Renovation of laboratory space
d. Change of the principal investigatora. Rebudgeting107.Federal Financial Assistance Management Improvement Act 1999 Public Law 106-107The impetus to change the ways in which federal agencies accept grant applications and manage grant awards has
108.The federal government prefers to disburse funds under federal grants via:
a. letters of credit
b. reimbursement check
c. electronic funds transfer
d. advanced treasury checksc. electronic funds transfer109.Federal regulations governing the use of humans in researchAlways require full informed consent of the subject or the subject's guardian110.The first $25,000When a subaward is involved in a federal grant to a large university, on what portion of the subawardee's budget does the prime institution recover facilities and administrative cost(indirect cost)?111.FOA instructions always supersede these form instructions.If you have a funding opportunity announcement (FOA), which instructions do you go by... the research form or the FOA112.For copyrighted works which result from federally sponsored activities the federal government usually requires
a. disclosure of the copyright only
b. one copy of the official archives
c. a royalty-bearing , exclusive, and irrevocable license
d. a royalty-free, nonexclusive, and irrevocable licenseb. one copy of the official archives113.Formulation of the President's Budget;
Action by the Congress; Presentation (to Congress) and-Execution of enacted budget lawsWhat are the 3 main phases in the Federal Budget Process114.Freedom of Information Act (FOI)What act brought this on FFATA?
115.From any institution that receives more than $700,000 in federal fundingUnder which of the following conditions is a Certificate of Current Cost and Pricing required116.The Fulbright Program provides opportunities for
a. teaching abroad
b. service abroad
c. teaching n low income communities
d. construction of low income housinga. teaching abroad117.Goals/Objectives/SOW/ImplementationApplicant should explain the expected results and benefits of each objectives.118.House of Representativesa provision or report language included primarily at the request of a Member, Delegate, Resident Commissioner, or Senator providing, authorizing or recommending a specific amount of discretionary budget authority, credit authority, or other spending authority for a contract, loan, loan guarantee, grant, loan authority, or other expenditure with or to an entity, or targeted to a specific State, locality or Congressional district, other than through a statutory or administrative formula driven or competitive award process.119.How does an institution find their DUNS numberYou can contact your office of sponsored research or you can also log in to the eRA Commons.
120.How many days do recipients of federal grant funds have to submit final reports after completion of the project period?
a. 30
b. 60
c. 90
d. 120c. 90121.How often do approved animal protocols need to be reviewed by the Institutional Animals Care and Use Committee (IACUC):
a. Annually
b. Semiannually
c. Every 2 years
d. Every 3 yearsd. Every 3 years122.How to do business internationallyThe Office of Commercial and Business Affairs (CBA) plays a major role in coordinating trade and investment matters to support U.S. firms doing business overseas. Our mission is to engage U.S. government resources to assist and promote U.S. business interests overseas, and to ensure that private sector business concerns are fully integrated into U.S. foreign and economic policy.123.iEdisonInteragency Extramural Invention Information Management System helps government grantees and contractors comply with a federal law, the Bayh-Dole Act regulations require that government funded inventions be reported to the federal agency who made the award
124.If a graduate student comes into a university sponsored research office charging that because of the federal Freedom on Information Act (FOIA) he has the right to obtain a copy of recently submitted proposal, the research administrator should
a. provide student with a complete copy of the proposal
b. provide student with a copy of the proposal with proprietary and salary information blacked out
c. advise student to apply to the federal agency to request a proposal 90 days after the proposal was submitted
d. tell the student to wait to apply to the federal agency until after the decision is made on the proposald. tell the student to wait to apply to the federal agency until after the decision is made on the proposal125.If an agency requires 20% cost sharing of the total project for a particular program and a proposal is requesting $200,000 from the agency, what is the additional amount that the institution must cost share?
a. $40,000
b. $50,000
c. $100,000
d. $220,000$50,000
$200000 / .8 = $250,000
$250,000-$200,000 = $50,000126.If an institution of higher education is subject to OMB Circular A-133, when must it have an independent audit?
a. Annually
b. Biennially
c. Triennially
d. At the discretion of its governing bodya. Annually127.If a principal investigator proposes to conduct research involving human subjects who will take a standardized educational test, but the test will not include any names or other identifying information, the proposal should be:
a. reviewed by the full Institutional Review Board
b. submitted for expedited review by the Institutional Review Board
c. submitted for review to the Office of Human Research Protection
d. treated under organization's policy as exempt from reviewb. submitted for expedited review by the Institutional Review Board
128.The impetus to change the ways in which federal agencies accept grant applications and manage grant awards has been mandated by:
a. e-Government strategies
b. new audit policies at the Office of Management & Budget
c. Office of Science & Technology Policy
d. the Federal Financial Assistance Management Improvement Act of 1999 (Public Law 106-107).d. the Federal Financial Assistance Management Improvement Act of 1999 (Public Law 106-107).129.indemnityOne may use what kind of clause to require that one party indemnify the other when certain expenses are incurred130.individual account in an approved accounting systemUpon receipt of awarded projects, educational institutions are required to establish131.Information is made available to the public by publication in the Federal Register, upon request given a description of the records desired and provides an opportunity to read and copy records at convenient locations.What is the Freedom of Information Act?132.In order for a foreign national student researcher to work on a federal grant in an American institution, it is necessary for the student to have:
a. a visa
b. United States citizenship
c. evidence of English proficiency
d. approval of student's embassya. a visa133.The Institutional Animal Care and Use Committee (IACUC) is required to inspect animal facilities a MINIMUM
a. one a month
b. twice a year
c. once a year
d. once every three yearsb. twice a year134.Institutional Biosafety CommitteeWhich of the following is mandated for the oversight of research involving recombinant DNA
135.Institutional National Research Service AwardsThe National Institutes of Health requires a written description of a program for providing instruction in the responsible conduct of research for136.The Institutional Official for a sponsored research projectThe individual authorized by the Board of Trustees to sign on behalf of the institution137.Institutions, InvestigatorsWho is covered by the COI regulation138.Institutions that have more than $25,000,000 in federal grants or contractsWhich of the following would be required to file a disclosure statement (DS-2) with the federal government?139.internal controlsEfficient and effective operations and reliable financial reporting are the objectives of140.International Traffic in Arms Regulations (ITAR) are controlled by the :
a. United Nations
b. U.S. Department of State
c. U.S. Department of Homeland Security
d. Bureau of Alcohol, Tobacco, and Firearmsb. U.S. Department of State141.In the credentials boxWhere do you put the ERA Login?142.In the event of cost overrun by a subcontractor, who would be held responsible by the funding sources?
a. Subcontractor only
b. Prime contractor only
c. Project director and subcontractor
d. Project directly and prime contractora. Subcontractor only
143.An investigator on an NIH grant has permission to rebudget $50,000 in supply monies into equipment. If the institution's facilities and administrative cost (indirect costs) rate (based on MTD) is 50%, how much money will be available for the equipment?
a. $25,000
b. $33,333
c. $50,000
d. $75,000d. $75,000
$50,000 X 1.50 = $75,000144.Involves a conflict of interestFaculty member is a major stockholder in a for profit company receiving a university contract145.Is a binding contract made between two parties, one of whom is the "Sponsor" or the company or individual sponsoring the clinical trial, while the other is the "Institution" or the organization or hospital receiving the sponsorship for conducting clinical trials.What is the Clinical Trial Agreement?146.Is intended to give credit where credit is due. Requires acknowledgement of Federal grant support when issuing statements, press releases, requests for proposals, bid solicitations, etc.What is the Stevens Amendment?147.is the grant of a property right to the inventor, issued by the Patent and Trademark Office. The term of a new patent is 20 years from the date on which the application was filedWhat is a patent?148.is to ensure that employers provide employees with an environment free from recognized hazards, such as exposure to toxic chemicals, excessive noise levels, mechanical dangers, heat or cold stress, or unsanitary conditions.What is the Occupational Safety & Health Act?149.Is usually riskier than a cost reimbursement contractWhich of the following best describes a fixed-price contract150.It is a public-private partnershipWhich of the following correctly describes FirstGov
151.It's required before an award at the proposal stage.If you don't have ERA Commons password, when is it required for an IRB?152.Judicial BranchCourts decide arguments about the meaning of laws and how they are applied. They also decide if laws violate the Constitution—this is known as judicial review, and it is how federal courts provide checks and balances on the legislative and executive branches.153."Just in time" initiatives postpone the submission of which of the following items until a decision to make an award is reached?
a. Full proposal
b. Budget justification
c. Certification and representations
d. Research background of principal investigatorc. certification and representations154.Land acquisitionIn a Construction Grant, which is allowable155.Law passed to protect certain species of marine mammals deemed as being in danger of extinctionWhat is the Marine Mammal Protection Act?156.Legislative BranchArticle I of the Constitution establishes the legislative or law making branch of government. It has a two-branch Congress—the Senate and the House of Representatives—and agencies that support Congress.157.Let SRO review the proposal then allow the PI to submitIf a federal agency requires a PI to submit online, what should be done158.Letter of supportA straight forward document stating that the institution is in support of the application to proceed and that it will host the proposed research should the application be successful.159.live, vertebrate animals onlyThe PHS policy governing the use and care of animals covers
160.Make sure budget/rates are accurate.If a PI submitted a proposal without going through the SRO office, what is our first concern?161.Mandates that a "Responsible Party" register and report results of certain "applicable clinical trials". Interventional studies of drugs, biologics, or devices that are subject to FDA regulations.What is the Food and Drug Administration Amendments Act (FDAAA)?162.Martial status of applicantUnder federal Equal Employment Opportunity provisions, a supervisor should NOT ask which of the following during an employment interview:163.Material Safety Data Sheet (MSDS) fileWhich of the following is essential to a Chemical Hygiene Plan?164.Material Transfer AgreementMTA165.Material transfer agreement (MTA)What is a contract that governs the transfer of tangible research materials between two organizations, when the recipient intends to use it for his or her own research purposes166.Material Transfer AgreementsRecommended so that disputes about use do not arise. __ are contractually binding upon the parties.167.A mechanism for procurement of a product or service with specific obligations for both sponsor and recipient. Designed to benefit the sponsor by achieving an expected outcome or product.What is a contract?168.Members of an Institutional Animal Care and Use Committee (IACUC) must be appointed
a. funding agency program officer
b. Office of Human Research Protection
c. responsible administrative official of the organization
d. research administrator responsible for the committeec. responsible administrative official of the organization
169.Member unaffiliated with the institutionAccording to federal regulations, which of the following must be included in an Institutional Review Board?170.minimum wages, maximum hours, child labor, convict labor and safe and sanitary working conditionsThe Walsh-Healey Public Contracts Act deals with issues on171.Modified total direct costIs a frequently used base for facilities and administrative cost (F&A) computation?172.modular budget is applicable only to R01, R03, R15, R21, and R34 applicationsIn an NIH Research Project Grant Program, which budget couldn't be over $25,000 in direct cost per year?173.The National Institutes of Health requires a written description of a program for providing instruction in the responsible conduct of research for:
a. program project grants
b. competing research project grants
c. noncompeting research project grants
d. Institutional National Research Service Awardsd. Institutional National Research Service Awards174.National Library of MedicineWhich of the following is located within the National Institutes of Health175.The National Science Foundation indicates decisions on the funding of grant proposals should normally takea
a. 2-4 months
b. 6-9 months
c. 10-12 months
d. 18-24 monthsb. 6-9 months176.Needs/Problem statementIt should be a clear and concise statement of the problem you want to solve with grant funds.
177.NIH: What are the main types of awardsResearch Grants (R series)
Career Development Awards (K series)
Research Training and Fellowships (T & F series)
Program Project/Center Grants (P series)178.NIH: What is Just-in-TimeRefers to the information that NIH will ask you to send after your application goes through initial peer review and is within the range of possible funding. NIH will need this information but does not require it with your application.179.Nondisclosure AgreementA Local Business wants to meet with a PI to discuss a product that they might agree to begin work on. What should be done?180.A Notice of Award typically includes which of the following?
a. Approval of facilities and administrative costs (Indirect Costs) rate
b. Award terms and conditions
c. Congressional approval
d. Guarantees for continuationb. Award terms and conditions181.Nuclear Regulatory CommissionStandards for handling radioactive materials are developed and monitored by the182.October 1The federal fiscal year begins:183.The Office and Grants and Contracts/Finance will monitor and draw cash on expenditures as appropriateThe university receives a grant from NIH that states the payment terms are DHHS Letter of Credit. This means:184.The office for Human Research Protection is administered by:
a. a private agency
b. a nonprofit foundation
c. an independent federal agency
d. a cabinet-level departmentd. a cabinet-level department
185.Office supplies, postage, administrative and clerical salaries, local telephone charges and general purpose equipmentThe following items should normally be treated as F&A cost except when the particular cost item can be justified as an exceptional need. What are some examples of exceptional need186.OMB Circular A-133The following establishes audit requirements and defines Federal responsibilities for implementing and monitoring these requirements for institutions of higher education and other nonprofit institutions receiving federal awards187.On an SF 424 Form, what does renewal, mean?requests additional funding for a period subsequent to that provided by a previous award and competes with all other applications.188.On an SF 424 Form, what does resubmission mean?has been previously submitted, but was not funded and is now being resubmitted.189.On an SF 424 Form, what does revision mean?proposes a change in 1) the Federal government's financial obligations or contingent liability from an existing organization, or 2) any other changes in the terms and conditions of the existing award, including requests for additional specific aims.190.Once each calendar year and is issued on a quarterly basisThe CFR is divided into 50 titles that represent broad areas subject to regulation and is published by the Federal executive agencies/departments. Each volume of the CFR is updated191.Payments to subjectsWhich of the following costs is allowable according to OMB Circular A-21?192.personnel salaries are increasedPrior approval from a federal agency is usually not needed when
193.The PHS policy governing the use and care of animals covers
a. live, vertebrate animals only
b. any animal use in research and training
c. animals involved in research only
d. animals that might otherwise be kept as pets onlya. live, vertebrate animals only194.PlagiarismThe appropriation of another person's ideas, processes, results, or words without giving appropriate credit195.A plan for expenditure of fundsWhich of the following must be included in every federal grant budget?196.Possible items could NIH request through Just-in-timeOther support Current and Pending, Certificate of IRB approval of proposed use of human subjects , Evidence of compliance with education in the protection of human subjects ,Verification of IACUC approval of proposed use of live vertebrate animals197.Primary purpose of a federal cooperative agreementTo provide assistance with substantial involvement of the federal agency198.prior actual costA facilities and administrative cost (indirect cost) rate is usually established based on
199.Prior approval from a federal agency is usually NOT needed when:
a. the scope of work is changed
b. personnel salaries are increased
c. the principal investigator is changed
d. additional alterations costing more than $10,000 are madeb. personnel salaries are increased200.Prior intramural support should be addressed in the narrativeWhen applying for extramural support, in which of the following ways should the principal investigator address prior related intramural support?201.PrisonersWhich of the following populations has special protection as research participants under federal guidelines?202.Prisoners, pregnant women, mentally unstable, and minors.Who cannot participate in clinical trials203.Privacy Act of 1974When an agency contracts for the design, development, or operation of a system of records on individuals on behalf of the agency to accomplish an agency function, the agency must apply the requirements of which of the following acts204.Project travelWhich of the following is NOT included in the computation of an indirect cost rate205.Proposal Central or Foundation web site.What resource site do Private Foundations mostly submitted through?206.Proposal SolicitationRFP and RFA are examples of207.protection provided to the authors of "original works of authorship" including literary, dramatic, musical, artistic, and certain other intellectual works, both published and unpublishedWhat is a copyright?208.protects certain health information and requires naming a Privacy Official and written policy and procedures.What is the Health Insurance Portability and Accountability Act (HIPPA) Patient Privacy Rule?
209.protects people from discrimination based on sex in education programs or activities which receive Federal financial assistanceWhat is Title IX of the Education Amendments: Sex Discrimination?210.Protects the rights of employees and employers. Encourages collective bargaining. And curtails certain private sector labor and management practices, which can harm the general welfare of workers, businesses and the US economy.What is the National Labor Relations Act?211.Provides an entitlement of up to 12 weeks of job-protected, unpaid leave funding any 12-month period for the following reasons; birth and care of the employees child, or placement for adoption or foster care of a child with the employees; care of an immediate family member who has a serious health condition or care of the employees own serious health condition.What is the Family and Medical Leave Act?212.Provides labor standards for certain persons employed by federal contractors over $2500 furnishing services to federal agencies.What is the Service Contract Act?213.Provisions are intended to help secure the nation against bioterrorism acts.The act requires individuals and institutions to nor produce, acquire, retain (stockpile) or possess types and quantities of any biological materials including bona fide research.What is the US Patriot Act?214.provisions for an organizational program for the care and use of animalsEach organization using animals in Public Health Service sponsored projects must provide written assurance of its compliance with215.RebudgetingFederal expanded authorities permit which of the following without additional sponsored approval?
216.received from any funding sourceCost Accounting Standards (CAS) must be applied to awards217.The recipient of federal funds agrees that US flag air carriers will be used to transport personnel and property when costs are charged to these funds including any air transportation to from between or within a country other than the US when US flag air carriers are available.What is the Fly America Act?218.Recipients of federal grant funds must retain records for a MINIUMUM of:
a. 180 days after closeout
b. 18 month after the grant end date
c. 2 years after each grant budget year
d. 3 years from submission of final report of expenditured. 3 years from submission of final report of expenditure219.Refer employee to appropriate institution representativeWhich of the following is an appropriate response to sexual harassment reported by an employee in the work force?220.Regular dissemination of funding opportunitiesWhich of the following is most important in developing a program of available support with a grantee institution?221.The Regulation imposes a 6-year time limitationWhat is the time limitation for occurrences of research misconduct to be brought to the attention of an institution or the Department of Health and Human Services (HHS) (see § 93.105)222.remain with the institutionUnder federal grant conditions, the title to equipment must223.RentWhich would you charge against F&A?224.Rental or usage fees from equipment purchased with grant fundsWhich of the following is considered program income?
225.Request a one year, no cost extension of the grant while a revised continuation is under preparationA faculty member has a five year National Institutes of Health (NIH) grant which will terminate August 31, with $14,000 remaining on July 15 of the same year. A competing continuation was recommended for approval but not funded. Which of the following is the most appropriate advice for the research administrator to give to the faculty member?226.Required information on federal awards be made available to the public via single, searchable websiteWhat is the Federal Funding Accountability and Transparency Act (FFATA)?227.Requires employers to assure that employees hired are legally authorized to work in the US.What is Immigration Reform and Control Act (IRCA)?228.Requires the government to show 3 materials elements on all sole source contracts with a the current threshold applicable to all agencies is $700,000 for prime contracts awardedWhat is Truth in Negotiations Act?229.Research misconductWhat is defined as fabrication, falsification and plagiarism, and does not include honest error or differences of opinion230.responsible administrative official of the organizationMembers of an Institutional Animal Care and Use Committee (IACUC) must be appointed by the231.Responsible Conduct of Research (RCR).What process was created from America COMPETES act?232.Restricts the political activity of executive branch employees of the federal government, District of Columbia government, and some state and local employees who work in connection with federally funded programsWhat is the Hatch Act?233.Returned to the sponsoring agencyUpon completion of a federal grant, excess funds remaining in the account should be
234.RFPWhich of the following would serve the purpose of inviting proposals and specifying the general terms and conditions under which the relevant award can be made235.Roles and responsibilities of the Principal Investigator and other key personnelProper technical conduct of the research effort
Compliance with the terms and conditions of the sponsored agreement, Managing project funds within the approved budget
Timely completion and submission of required technical reports
Complying with all university and sponsor policies and procedures pertinent to the award236.Roles and responsibilities of the Sponsored Programs OfficeProviding accounting, Purchasing
Other administrative services to assist the principal investigators in: - managing the financial aspects of their projects
obtaining the necessary goods, services, and personnel to conduct the research effort, meeting sponsor needs for fiscal reports, Provides financial accounting to sponsors for the activity funded and is subject to federal audit.237.a royalty-free, nonexclusive, and irrevocable licenseFor copyrighted works which result from federally sponsored activities, the federal government usually requires238.Salaries and wagesWhich of the following is a base for facilities and administrative cost (indirect rate)?239.Salary or other payments for service, equity interests, intellectual property rights.Significant Financial Interest is defined by the regulation as anything of monetary value, including but not limited to:240.SF269The following is used to prepare quarterly, semi-annual, annual, or end reports241.SF270The following is used to request for an advance or reimbursement242.SF272The following is used to prepare a report of federal cash transactions243.Shelby AmendmentAccess to federally funded research data is required under the244.Should be closely followedWhich of the following is most appropriate use of federal agency guidelines for writing a proposal245.SponsorWhich of the following is responsible for clinical trial registration on ClinicalTrials.gov?
246.Standards for handling radioactive materials are developed and monitored by the:
a. Nuclear Regulatory Commission
b. Environmental Protection Agency
c. Centers for Disease Control and Prevention
d. Occupational Safety and Health Administrationa. Nuclear Regulatory Commission247.State and local governments are subject to which of the following OMB Circulars?
a. 2 CFR 220 (A-21)
b. A-102
c. 2 CFR 230 (A-122)
d. A-133b. A-102248.Subcontractor onlyIn the event of a cost overrun by a subcontractor, who would be held responsible by the funding source?249.Subcontractor's normal rateWhich of the following establishes the actual facilities and administrative cost (indirect cost) rate for a subcontract?250.Subcontract, Subgrant, or SubagreementA document written under the authority of, and consistent with the terms and conditions of an award, that transfers a portion of the research of substantive effort of the prime award to another institution or organization.251.System for Award Management (SAM)What is the name of the system for requiring submission and maintenance of representations and certifications252.Task Order Agreement TOAA legally binding document authorizing work and appropriating funds as a supplement to a basic contact.
253.teaching abroadThe Fulbright Program provides opportunities for254.Teaming AgreementAn agreement between two or more parties to participate in a research project or teaching activity255.Temporary rate subject to final negotiationWhich of the following best describes a provisional indirect cost rate256.They upload it to their submission application. Not on the SF 424 formIf a PI wants to request a reviewer to a proposal submission, where can they do this257.TitleIt should tell us in 25 words or less what you intend to research and should be relevant258.TravelWhich of the following expenses would be included in the distribution base of modified total direct costs?259.The travel costs do not provide any benefit to the federally sponsored projectA PI on a federally awarded grant wants to charge travel costs to a project for attendance at a conference that is unrelated to the project. Which of the following BEST explains why the PI cannot charge the travel costs to the project260.treated under organization's policy as exempt from reviewIf a principal investigator proposes to conduct research involving human subjects who will take a standardized educational test, but the test will not include any names or other identifying information, the proposal should be261.TrueUBMTA may not be usable for materials in projects supported by industry. True or False262.TrueA one-time no-cost extension up to 12 months is allowed as an expanded authority. True or False263.twice a yearThe Institutional Animal Care and Use Committee (IACUC) is required to inspect animal facilities a MINIMUM of
264.Under a federal contract, which of the following is a reason for termination for default?
a. Untimely performance
b. Budget revision
c. Cost overrun
d. Inadequate performance on another contracta. Untimely performance265.Under federal grant conditions, the title to equipment must
a. remain with the agency
b. remain with the institution
c. be vested with the institution only under $5,000
d. be vested in the institution with the agency's right to transfer to itself or another entityb. remain with the institution266.Under which of the following conditions is a Certificate of Current Cost and Pricing required?
a. For a federal contract over $1,000,000
b. For any federal subcontractor
c. From any institution that received more than $500,000 in federal funding
d. As a standard of certification submitted by institutions applying for federal grantsc. from an institution that received more than $500,000 in federal funding267.Uniform Biological Material Transfer Agreement (UBMTA)Makes one class of transfers routine
Standard terms developed in 1995 by NIH sponsored group
Provides standardized approach for certain transfers between academic institutions
268.Unilateral AwardAn award made by a sponsored to an organization without considering competitive proposals. They are most often made when unsolicited proposals receive favorable treatment.269.United States Department of Agriculture (USDA)is the U.S. federal executive department responsible for developing and executing federal government policy on farming, agriculture, forestry, and food. It aims to meet the needs of farmers and ranchers, promote agricultural trade and production, work to assure food safety, protect natural resources, foster rural communities and end hunger in the United States and abroad.270.United States Department of Homeland Securitya cabinet department of the United States federal government, created in response to the September 11 attacks, and with the primary responsibilities of protecting the United States and its territories (including protectorates) from and responding to terrorist attacks, man-made accidents, and natural disasters.271.United States Department of Veterans Affairsis a government-run military veteran benefit system with cabinet-level status. It is the United States government's second largest department, after the United States Department of Defense.272.unlike circumstances are presentA facilities and administrative cost (indirect cost) may be a direct cost if273.Untimely performanceUnder a federal contract, which of the following is a reason for termination for default?
274.Upon completion of a federal grant, excess funds remaining in the account should be :
a. returned to the sponsoring agency
b. transferred to another sponsored project
c. assigned to institution's general funds
d. included in proposal for an additional granta. returned to the sponsoring agency275.Upon receipt of awarded projects, educational institutions are required to establish?
a. credit card account for the investigator
b. combined accounts for easier investigator access
c. noninstitutional savings account for the investigators
d. individual accounts in an approved accounting systemd. individual accounts in an approved accounting system276.U.S. Department of Justice, under the False Claims ActWhich federal agency is responsible for prosecuting institutional violations of effort reporting277.U.S. Department of StateInternational Traffic in Arms Regulations (ITAR) are controlled by the278.Using the criteria contained in 2 CFR 220 (OMB Circular A-21), which of the following costs would most likely be allowable as a direct expenditure item on a federal grant?
a. Costs of preparing the grant proposal
b. Break refreshments at a project-sponsored workshop
c. Facility rental for a project staff holiday party
d. An amount specifically set aside for unanticipated expensesb. Break refreshments at a project-sponsored workshop279.Varies with funding sourceFederal regulations require that documentation of expenditures must be kept for how long?280.verifiable from recordsCost sharing must be
281.A vivariumWhat is an area, usually enclosed, for keeping and raising animals or plants for observation or research282.What are allowable costsAre costs that can be legitimately charged to a grant. An award refers to those funds that have been obligated by a funding agency for a specific project.283.What are Research Administrators?Advocate, Facilitator, Gatekeeper, Reviewer, Enforcer, Motivator, Resource Locator, Interpreter,Team Builder,Compliance Manager284.What are the roles and responsibilities of the InstitutionExpedite hiring of staff and faculty to enable work to proceed from the start of the award; Assist departments, schools, the Office of Research, and the Office of Research Accounting to facilitate administrative tasks; Meet the terms and conditions of the sponsored award in collaboration with the Investigators;-Provide timely and accurate monthly accounting reports to Investigators285.What determines if Financial Interest is SignificantFunds received for investigator and spouse/children meets both the following tests: 1) does not exceed $5000 in value as determined through reference to public prices or other reasonable measures of market value 2) does not represent more than a 5% ownership interest in any single entities.286.What is a Commercial And Government Entity Code (CAGE) and its purposeis a unique identifier assigned to suppliers to various government or defense agencies, as well as to government agencies themselves and also various organizations. It provide a standardized method of identifying a given facility at a specific location.287.What is a Data Universal Numbering System (DUNS Number)?is a system developed and regulated by Dun & Bradstreet that assigns a unique numeric identifier to a single business entity. That number is a nine-digit number issued to each business location in the D&B database having a unique, separate, and distinct operation for the purpose of identifying them.288.What is a grant?A type of financial assistance awarded for the conduct of research and no substantial programmatic involvement with the recipient during the performance of the activities.289.What is an Invitation For Bid (IFB)?the method used for the sealed bid process. A contract is then awarded to the low bidder whose bid conforms with all requirements of the invitation and will be advantageous to the government in terms of price, and price-related factors
290.What is a Request for Proposal (RFP)?occurs when the agency isn't certain about what it wants and is looking to you to develop a solution and cost estimate.291.What is a Request for Quote (RFQ)is often used to determine current market pricing, but is not a binding offer and can't be accepted by the government. A Standard Form 26, which requires the signatures of both the contractor and the contracting officer, would be required to make the offer binding.292.What is a Student Visa?Generally, a citizen of a foreign country who wishes to enter the United States must first obtain a visa, either a nonimmigrant visa for temporary stay, or an immigrant visa for permanent residence. You must have a student visa to study in the United States. Your course of study and the type of school you plan to attend determine whether you need an F-1 visa (academic) or an M-1 visa (vocational).293.What is Catalog of Federal Domestic Assistance (CFDA)?is a government-wide compendium of an online database listing all available federal programs.294.What is debarment?removes you as a contractor from eligibility for future government contracts for a fixed period of time.295.What is Drug Free Work ForceDOD contractors must maintain records regarding drug-free work force programs provided to their employees. Also establishes a program testing for the use of illegal drugs by employees.296.What is effort reportingThe percentage of total employment devoted to a particular project, activity, administrative task297.What is Equal Employment Opportunity?provide equal opportunity without regard to race, color, religion, sex, or nationality to persons employed or seeking employment298.What is Fair Labor Standards Act?Enacted to establish a minimum hourly wage, overtime pay and regulate child labor299.What is Health Resources and Services Administration (HRSA) and who do they fall underimproves access to healthcare for people who are uninsured, isolated, or medically vulnerable and under DHHS.
300.What is Lobbyingthe act of attempting to influence decisions made by officials in the government, most often legislators or members of regulatory agencies.301.What is Small Business Innovative Research (SBIR)?refers to the agency administered programs that are supported by ear-marked federal funds, making grants to small business entities302.What is Small Business Technology Transfer (STTR)?refers to the grant applications and/or programs for funding those small business that are teamed up with research institutions.303.What is suspension?temporarily debars a contractor for the duration of any agency investigation of the contractor or ensuing legal proceedings.304.What is the America COMPETES Act?America Creating Opportunities to Meaningfully Promote Excellence in Technology, Education and Science- focuses on increasing research investment
Strengthens STEM Research (science, technology, engineering and math) from elementary through grad school.305.What is the Buy America Act?Establish a general preference for domestic articles, materials/supplies to protect the American worker by saving and creating jobs.306.What is the Byrd Amendment?Institution must certify that no appropriated funds were or will be expended to pay any person for influencing or attempting to influence an officer or an employee of any agency, a member of Congress, an officer or employee of Congress in connection with a specific award.307.What is the Civil Rights Act?Bars recipients of federal funds from excluding persons because of race, sex, color, or national origin from participation in receiving benefits or otherwise subjecting them to discrimination under federally supported programs or activities. Law also interpreted to cover discrimination against those persons with limited English. Sex includes pregnancy, childbirth or related medical conditions.308.What is the Confidentiality of Patient Records?Enacted to protect persons with substance abuse problems who seek treatment.309.What is the Davis/Bacon ActRequires contractors to pay wages to laborers and mechanics at a rate of no less than a minimum wage specified in a wage determination made by the Secretary of Labor.
310.What is the Drug Free Workplace ActIt says you can't receive federal funding if you do not have a drug-free workplace policy in place311.What is the Endangered Species Act?species listed as endangered or threatened prohibits the unauthorized taking, possession, sale and transport of those species312.What is the Equal Pay Act?act prohibits employers and unions from paying different wages based on the employees sex313.What is the False Claims Act?Improper costing, product substitutions, failure to comply with contract specifications and filing false claims with government health care programs314.What is the percentage that all STTR budgets must matchAt least 40 percent of the STTR research project is to be conducted by the small business concern and at least 30 percent of the work is to be conducted by the single "partnering" research institution.315.What is the Ruth L. Kirschstein NSRA Award? Why is it importanttrain fellows and residents, and are used to promote the education of future researchers. She was a champion of research training and a strong advocate for the inclusion of underrepresented individuals in the scientific workforce316.What is the Solomon Act (Amendment)/ National Defense Authorization ActWhat United States federal law that allows the Secretary of Defense to deny federal grants (including research grants) to institutions of higher education if they prohibit or prevent ROTC or military recruitment on campus.317.What is use of name exceptionIt's an exception that agree that neither party will use directly or by implication names or trademarks of the other party in connection with any publicity, promotion or advertising without prior written approval.318.What is voluntary committed cost sharing?when the proposing institution volunteers and commits to bear a specific portion of the costs of the project when it is not required.319.What is voluntary uncommitted cost sharing?when the PI chooses to expend some unspecified amount of effort more than proposed towards the award. This is usually the case when the PI is not requesting salary from the award, and so is volunteering his/her effort.
320.When applying for extramural support, in which of the following ways should the PI address prior related support?
a. Prior intramural support should be ignored
b. Prior intramural support can be considered as an item of cost sharing in the budget narrative
c. Prior research related support should be considered unrelated in current grant request
d. Prior intramural support should be addressed in the narratived. Prior intramural support should be addressed in the narrative321.When a subaward is involved in a federal grant to a large university, on what portion of the subawardee's budget does the prime institution recover facilities and administrative costs (indirect costs)?
a. None of it
b. The first $25,000
c. The subawardee's modified total direct cost amount
d. The amount is excess of $25,000b. The first $25,000322.Whenever covered animals are involved in a protocolWhich of the following requires Institutional Animal Care and Use Committee (IACUC) review and approval governing the use of animals?323.When granted expanded authorities pre-award costs on a federal grant may be incurred by an institutional within
a MAXIMUM of how many days prior to the official start date:
a. 30 days
b. 45 days
c. 90 days
d. 120 daysc. 90 days
324.Which federal agency is responsible for prosecuting institutional violations of effort reporting?
a. U.S. Department of Justice, under the False Claims Act
b. Government Accountability Office, under the Code of Federal Regulations
c. Office of Management and Budget, under OMB Circular A-133 Audit Requirements
d. National Science Foundation Office of the Inspector General, under Congressional Oversight Authoritya. U.S. Dept of Justice, under the False Claims Act325.Which of the following agencies does NOT fund health science research?
a. U.S. Army
b. Department of Energy
c. National Institute of Aging
d. National Science Foundationd. National Science Foundation326.Which of the following agencies is responsible for administering the Animals Welfare Act?
a. Public Health Service
b. Department of Agriculture
c. Environmental Protection Agency
d. American Society for Prevention of Cruelty to Animalsb. Department of Agriculture327.Which of the following are two critical termination clauses of General Provisions of a federal contract:
a. Dispute and changes
b. Default and convenience
c. Default and stop work order
d. Stop work order and failure to confirmb. Default and convenience
328.Which of the following best describes 2 CFR 220 (OMB Circular A-21)?
a. Is applicable only to NSF and NIH
b. Allows federal agencies to places additional restrictions on individual items of costs
c. Deals with cost determination but does not identify the circumstances or dictate the participation in the financing of a project
d. Establishes principles for determining costs applicable to contracts, grants, and other agreements with both educational institutions and hospitalsc. Deals with cost determination but does not identify the circumstances or dictate the participation in the financing of a project329.Which of the following best describes federal regulations governing the use of humans in research?
a. Allow the researcher full discretion as to what to include in informed consent materials
b. Always require full informed consent on the subject or the subject's guardian
c. Allow the Institutional Review Board discretion in limited situations to approve protocols providing less than full informed consent
d. Waive full informed consent of the subject when the protocol is too complicated for an individual subject to understand the risksb. Always require full informed consent on the subject or the subject's guardian330.Which of the following delegates to grantee authorization of one year, no-cost extensions?
a. Expanded Authorities
b. Cost Accounting Standards
c. Public Law 106-107
d. Code of Federal Regulationsa. Expanded Authorities331.Which of the following establishes the actual facilities and administrative cost (indirect cost) rate for a subcontract?
a. Prime recipient's rate
b. Prime award agreement
c. Subcontractor's normal rate
d. Agreement between subcontractor and funding agencyc. Subcontractor's normal rate
332.Which of the following expenses would be include in the distribution base of modified total direct costs?
a. travel
b. equipment depreciation
c. sponsored programs office expenses
d. the portion of each subcontract in excess of $25,000b. equipment depreciation333.Which of the following information must be included in the notification by a federal officer to the contractor to terminate a contract for convenience?
a. Signature of program office
b. The effective date of the contract
c. A citation of the contract clause authorizing the termination
d. A specific statement defining the reason for the termination noticed. A specific statement defining the reason for the termination notice334.Which of the following involves a conflict of interest?
a. Faculty member owns and operates a business outside of university commitment
b. Faculty member consults with outside business in area of expertise
c. Faculty member supervises students employs them in university sponsored projects
d. Faculty member is a major stockholder in a for-profit company receiving a university contractd. Faculty member is a major stockholder in a for-profit company receiving a university contract335.Which of the following is a base for facilities and administrative costs (indirect costs)?
a. Subcontracts
b. Capital Equipment
c. Salaries and wages
d. Professional and outside servicesc. Salaries and wages336.Which of the following is a frequently used base for facilities and administrative costs (indirect cost) computations
a. Nonsalary costs
b. Capitalized equipment
c. Modified total direct cots
d. Total direct costs less pre-award costsc. Modified total direct cots
337.Which of the following is allowable as cost sharing?
a. Equipment donated at fair market value
b. Alcohol purchased for an allowable business dinner
c. A portion of the salary of the department head's secretary
d. Travel costs in excess of institutional per diema. Equipment donated at fair market value338.Which of the following is a primary purpose of a federal cooperative agreement?
a. To allow for flexible budgeting
b. To provide assistance with few restrictions
c. To enable solicitation by a Request of Proposal
d. To provide assistance with substantial involvement of federal agencyd. To provide assistance with substantial involvement of federal agency339.Which of the following is essential to a Clinical Hygiene Plan?
a. Material Safety Data Sheet (MSDS) file
b. Monthly fire and safety drills
c. Public information program
d. Federal Food & Drug Administration inspectiona. Material Safety Data Sheet (MSDS) file340.Which of the following is included in 2 CFR 215 (OMB Circular A-110)?
a. Audit requirements
b. Debarment and suspension rules
c. Federal contact requirements
d. Cost principles for nonprofitsb. Debarment and suspension rules341.Which of the following is located within the National Institutes of Health?
a. National Library of Medicine
b. Centers for Disease Control and Prevention
c. Food and Drug Administration
d. National Institute for Occupational Safety and Healtha. National Library of Medicine
342.Which of the following is mandated for the oversight of research involving recombinant DNA?
a. rDNA Committee
b. Biosafety Ethics Committee
c. Institutional Biosafety Committee
d. Institutional Biohazard Committeec. Institutional Biosafety Committee343.Which of the following is most important in developing a program of available support within a grantee institution?
a. Hiring of information specialist
b. Regular dissemination of funding opportunities
c. Development of subject-related database
d. Establishment of potential investigator fileb. Regular dissemination of funding opportunities344.Which of the following is responsible for clinical trail registration of Clinical Trials.gov?
a. Sponsor
b. Institution
c. Sponsored research office
d. Institutional Review Board (IRB)a. Sponsor345.Which of the following populations has special protection as research participates under federal guidelines?
a. Elderly
b. Prisoners
c. College Students
d. Persons diagnosed as HIV positiveb. Prisoners346.Which of the following requires Institutional Animal Care and Use Committee (IACUC) review and approval governing the use of animals?
a. When any animal is used
b. Only when laboratory animals are used in instruction
c. Whenever covered animals are involved in a protocol
d. Only if a protocol involve sacrificing animalsc. Whenever covered animals are involved in a protocol347.Which of the following sources in NOT commonly used for FEDERAL funding opportunites:
a. The Federal Register
b. The Foundation Directory
c. Commerce Business Daily
d. The Catalog of Federal Domestic Assistanceb. The Foundation Directory
Take courses from CCRPS and learn more on how to become a clinical research professional.
Here are some courses you might consider:
Clinical Research Coordinator Certification - Ideal for those looking to coordinate clinical trial activities.
Pharmacovigilance Certification - Focuses on drug safety and adverse effects management.
CRA Certification - Prepares you for the role of Clinical Research Associate.
ICH-GCP Certification - Essential for professionals needing to understand Good Clinical Practice guidelines.
Clinical Trials Assistant Training - Provides foundational knowledge for those starting in clinical trials.
Advanced Clinical Research Project Manager Certification - For experienced professionals aiming for project management roles.
Advanced Principal Investigator Physician Certification - Tailored for physicians leading clinical trials.
Medical Monitor Certification - Designed for those overseeing the medical aspects of clinical trials.
Discover more from Clinical Research Training | Certified Clinical Research Professionals Course
2018 Clinical Research Associate (CRA) Salaries Estimated from 1,850 American Employees
Skills Alliance Clinical Research Associate
Clinical Research Associate Job available
$113,368 per year
Advanced Clinical Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$107,750 per year
Syneos Health Commercial Solutions Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$98,894 per year
Piper Companies Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$101,820 per year
Novella Clinical Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$97,659 per year
Covance Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$96,667 per year
Premier Research Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$95,178 per year
Syneos Health Clinical Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$93,469 per year
PRA Health Sciences Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$76,150 per year
Novo Nordisk, Inc. Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$95,242 per year
PPD Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$91,293 per year
IQVIA Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$89,615 per year
Cyberonics Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$87,000 per year
AbbVie Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$81,391 per year
ICON plc Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$79,110 per year
PAREXEL Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$81,281 per year
QuintilesIMS Clinical Research Associate
11 salaries
Clinical Research Associate Job available
$72,749 per year
MD Anderson Cancer Center Clinical Research Associate
7 salaries
Clinical Research Associate Job available
$71,410 per year
Chiltern International Clinical Research Associate
5 salaries
$87,722 per year
Skills Alliance Clinical Research Associate - CRA Course
Clinical Research Associate Job available - CRA Course
$113,368 per year
Advanced Clinical Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$107,750 per year
Syneos Health Commercial Solutions Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$98,894 per year
Piper Companies Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$101,820 per year
Novella Clinical Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$97,659 per year
Covance Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$96,667 per year
Premier Research Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$95,178 per year
Syneos Health Clinical Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$93,469 per year
PRA Health Sciences Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$76,150 per year
Novo Nordisk, Inc. Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$95,242 per year
PPD Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$91,293 per year
IQVIA Clinical Research Associate - CRA Course
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$89,615 per year
Cyberonics Clinical Research Associate
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$87,000 per year
AbbVie Clinical Research Associate - CRA Course
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$81,391 per year
ICON plc Clinical Research Associate - CRA Course
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$79,110 per year
PAREXEL Clinical Research Associate - CRA Course
Requires CCRP Online CRA Training Program Certification (Completed in 4 Weeks; you can apply 2 weeks into the course).
Clinical Research Associate Job available
$81,281 per year
QuintilesIMS Clinical Research Associate - CRA Course
11 salaries
Clinical Research Associate Job available
$72,749 per year
MD Anderson Cancer Center Clinical Research Associate - CRA Course
7 salaries
Clinical Research Associate Job available
$71,410 per year
Chiltern International Clinical Research Associate - CRA Course
5 salaries
$87,722 per year
Pharmanet Clinical Research Associate - CRA Course
5 salaries
$72,488 per year
Roche Clinical Research Associate - CRA Course
5 salaries
Clinical Research Associate Job available
$71,586 per year
University of Florida Clinical Research Associate - CRA Course
11 salaries
Clinical Research Associate Job available
$69,492 per year
Department of Veterans Affairs Clinical Research Associate - CRA Course
6 salaries
Clinical Research Associate Job available
$66,274 per year
Abbott Laboratories Clinical Research Associate - CRA Course
6 salaries
Clinical Research Associate Job available
$66,095 per year
University of Utah Clinical Research Associate - CRA Course
19 salaries
Clinical Research Associate Job available
$66,775 per year
University of Minnesota Clinical Research Associate - CRA Course
8 salaries
Clinical Research Associate Job available
$64,600 per year
University of Connecticut Health Center Clinical Research Associate - CRA Course
8 salaries
Clinical Research Associate Job available
$58,321 per year
St. Jude Children's Research Hospital Clinical Research Associate - CRA Course
6 salaries
Clinical Research Associate Job available
$56,315 per year
Northwestern University Clinical Research Associate - CRA Course
6 salaries
Clinical Research Associate Job available
$54,342 per year
Duke Clinical Research Institute Clinical Research Associate - CRA Course
5 salaries
$73,447 per year
Emory University Clinical Research Associate - CRA Course
5 salaries
Clinical Research Associate Job available - CRA Course
$50,778 per year
Medpace Clinical Research Associate
6 salaries
Clinical Research Associate Job available
$50,958 per year
University of South Florida Clinical Research Associate
20 salaries
Clinical Research Associate Job available
$50,810 per year
The University of Iowa Clinical Research Associate
26 salaries
Clinical Research Associate Job available
$43,547 per year
Yale University Clinical Research Associate
5 salaries
Clinical Research Associate Job available
$40,378 per year
University of Maryland, Baltimore Clinical Research Associate
7 salaries
Clinical Research Associate Job available
$39,818 per year
University of North Carolina at Chapel Hill Clinical Research Associate
7 salaries
Clinical Research Associate Job available
$38,402 per year
University of North Carolina at Greensboro Clinical Research Associate
5 salaries
Clinical Research Associate Job available
$38,475 per year
Virginia Commonwealth University Clinical Research Associate
19 salaries
Clinical Research Associate Job available
$36,453 per year
University of North Carolina Clinical Research Associate
15 salaries
$36,955 per year
University of Pittsburgh Clinical Research Associate
13 salaries
Clinical Research Associate Job available
$33,878 per year
SUNY Downstate Medical Center Clinical Research Associate
9 salaries
Clinical Research Associate Job available
$33,343 per year
Washington University in St. Louis Clinical Research Associate
18 salaries
Clinical Research Associate Job available
$15.75 per hour
UC San Diego Clinical Research Associate
19 salaries
Clinical Research Associate Job available
$4,353 per month
University of California - San Francisco Clinical Research Associate
6 salaries
Clinical Research Associate Job available
$100 per day
Real Staffing Clinical Research Associate
15 salaries
Clinical Research Associate Job available
$31.95 per hour
University of Nebraska Medical Center Clinical Research Associate
12 salaries
Clinical Research Associate Job available
$15.81 per hour
Texas Tech University Health Sciences Center Clinical Research Associate
6 salaries
Clinical Research Associate Job available
$3,609 per month
Aerotek Clinical Research Associate
8 salaries
$47.68 per hour
Randstad Clinical Research Associate
35 salaries
$45.90 per hour
Ohio State University Clinical Research Associate
124 salaries
Clinical Research Associate Job available
$14.49 per hour
University of Kentucky Clinical Research Associate
59 salaries
Clinical Research Associate Job available
$21.63 per hour
Biotech Partners Clinical Research Associate
12 salaries
Clinical Research Associate Job available
$111,431 per year
DOCS Global Clinical Research Associate
14 salaries
Clinical Research Associate Job available
$90,856 per year
CyberCoders Clinical Research Associate
28 salaries
$88,409 per year
Zp group Clinical Research Associate
18 salaries
$98,008 per year
CIG Clinical Research Associate
109 salaries
$116,784 per year
CorTech, LLC Clinical Research Associate
40 salaries
$38.91 per hour
Skills Alliance (Recruiting Company) Clinical Research Associate
12 salaries
$71.01 per hour
InfoStaff Clinical Research Associate
52 salaries
$109,699 per year
Stony Brook University Clinical Research Associate
5 salaries
Clinical Research Associate Job available
$39,254 per year
Brio Resource Group Clinical Research Associate
46 salaries
Clinical Research Associate Job available
$129,987 per year
Planet Pharma Clinical Research Associate
7 salaries
Clinical Research Associate Job available
$117,458 per year
biorasi LLC Clinical Research Associate
18 salaries
$63,702 per year
Intermountain Home Care Clinical Research Associate
11 salaries
$15.55 per hour
Piper Clinical Solutions Clinical Research Associate
16 salaries
$64,853 per year
Personify Clinical Research Associate
36 salaries
$99,373 per year
Segal Trials Clinical Research Associate
24 salaries
$2,195 per month
Bertram & Associates Clinical Research Associate
7 salaries
$116,417 per year
Lodestar Executive Search Clinical Research Associate
7 salaries
$116,417 per year
PSU Personnel Services Unlimited, Inc. Clinical Research Associate
6 salaries
$104,485 per year
The Hastings Group Clinical Research Associate
7 salaries
$116,417 per year
Ploeger Recruiting Services Clinical Research Associate
6 salaries
$104,485 per year
Phillips Staffing Solutions Clinical Research Associate
6 salaries
$104,485 per year
PMG Employment Consultants Clinical Research Associate
7 salaries
$116,417 per year
Bio-Partners Clinical Research Associate
7 salaries
$116,417 per year
Hire Horizons Clinical Research Associate
6 salaries
$104,485 per year
SearchStars Clinical Research Associate
6 salaries
$104,485 per year
Fowler Placement Services, Inc. Clinical Research Associate
6 salaries
$104,485 per year
Plastic Executive Recruiters Clinical Research Associate
6 salaries
$104,485 per year
EPM Scientific Clinical Research Associate
13 salaries
Clinical Research Associate Job available
$98,268 per year
Barrington James Clinical Research Associate
12 salaries
Clinical Research Associate Job available
$124,820 per year
MedExec International Clinical Research Associate
6 salaries
$104,485 per year
Tri-Force Clinical Research Associate
7 salaries
$116,417 per year
Professional Recruiting Partners, LLC Clinical Research Associate
7 salaries
$116,417 per year
Career Brokers, Inc. Clinical Research Associate
6 salaries
$104,485 per year
Helffrich International Clinical Research Associate
6 salaries
$104,485 per year
Tailored Management Clinical Research Associate
10 salaries
$79,138 per year
MJ Recruiters, LLC Clinical Research Associate
6 salaries
$104,485 per year
Meet Recruitment Clinical Research Associate
12 salaries
$102,820 per year
University of Virginia Clinical Research Associate
16 salaries
Clinical Research Associate Job available
$44,455 per year
Medical University of South Carolina Clinical Research Associate
20 salaries
Clinical Research Associate Job available
$32,233 per year
Oregon Health Sciences University Clinical Research Associate
17 salaries
Clinical Research Associate Job available
$43,176 per year
AutoPro Technical Recruiting Clinical Research Associate
6 salaries
$104,485 per year
MMS Group Clinical Research Associate
6 salaries
$104,485 per year
ONESource Technical Clinical Research Associate
6 salaries
$104,485 per year
Technology Recruiting Solutions, Inc. Clinical Research Associate
6 salaries
$104,485 per year
BRUNEL CANADA Clinical Research Associate
20 salaries
$83,573 per year
Affinity Executive Search Clinical Research Associate
20 salaries
$111,284 per year
PPD Development, L.P. Clinical Research Associate
11 salaries
$92,737 per year
HireNetworks Clinical Research Associate
12 salaries
Clinical Research Associate Job available
$94,478 per year
CMC Limited Clinical Research Associate
13 salaries
$111,719 per year
CMD And Associates Clinical Research Associate
17 salaries
$97,982 per year
fulltimeGiGS Clinical Research Associate
10 salaries
$120,496 per year
Cameron Craig Group Clinical Research Associate
17 salaries
$88,715 per year
Prevalent Group Clinical Research Associate
17 salaries
$95,522 per year
True North Consultants Clinical Research Associate
6 salaries
$104,485 per year
Financially Stable Pharmaceutical Clinical Research Associate
8 salaries
$112,472 per year
JDP Search Group Clinical Research Associate
16 salaries
$99,326 per year
PeopleStaff Clinical Research Associate
15 salaries
$84,270 per year
Clinical Management Consultants Clinical Research Associate
9 salaries
Clinical Research Associate Job available
$115,881 per year
JOHNLEONARD Clinical Research Associate
8 salaries
Clinical Research Associate Job available
$61,509 per year
Rangam Consultants Inc. Clinical Research Associate
5 salaries
Clinical Research Associate Job available
$72,617 per year
Keshav Consulting Solutions Clinical Research Associate
13 salaries
$60,670 per year
Onboard.jobs Clinical Research Associate
15 salaries
$94,156 per year
Cor-Tech LLC Clinical Research Associate
15 salaries
$42.97 per hour
Klinexa Inc. Clinical Research Associate
8 salaries
$25.00 per hour
Systematic business consulting Clinical Research Associate
13 salaries
$88,299 per year
University of Miami Miller School of Med Clinical Research Associate
8 salaries
$74,809 per year
Global Channel Management, Inc. Clinical Research Associate
12 salaries
$41.26 per hour
Productive Data Solutions, INC. Clinical Research Associate
8 salaries
Clinical Research Associate Job available
$27.00 per hour
Selective Staffing Solutions Clinical Research Associate
8 salaries
Clinical Research Associate Job available
$19.49 per hour
Atlanta Center for Medical Research Clinical Research Associate
5 salaries
$33,642 per year
DOCS Clinical Research Associate
10 salaries
$78.22 per hour
Impact Business Group Clinical Research Associate
12 salaries
$54.45 per hour
CPS Recruitment Clinical Research Associate
7 salaries
$28.46 per hour
SCOPE International USA, Inc. Clinical Research Associate
11 salaries
$80,886 per year
Interview with Center for Advanced Obstetrical Care and Research Clinical Research Associate
8 salaries
$17.00 per hour
Inflamax Research Inc. Clinical Research Associate
6 salaries
$2,900 per month
Priority Sales Recruiting Clinical Research Associate
11 salaries
$108,226 per year
University of Texas Medical Branch Clinical Research Associate
5 salaries
Clinical Research Associate Job available
$16.50 per hour
Eastern Virginia Medical School Clinical Research Associate
10 salaries
Clinical Research Associate Job available
$82,730 per year
Computech Corporation Clinical Research Associate
7 salaries
$45.00 per hour
Details on application Clinical Research Associate
9 salaries
$205,058 per year
BK Rich Associates Clinical Research Associate
6 salaries
$90,000 per year
Central Florida Careers Clinical Research Associate
9 salaries
$16.93 per hour
Chipton Ross Clinical Research Associate
10 salaries
$34.37 per hour
AppleOne Clinical Research Associate
10 salaries
$75,534 per year
Sabio Systems Clinical Research Associate
9 salaries
$19.90 per hour
Blair Search Clinical Research Associate
7 salaries
$116,417 per year
Sponsor Pharmaceutical company Clinical Research Associate
9 salaries
$110,000 per year
Helix Biomedics LLC Clinical Research Associate
6 salaries
$12.00 per hour
Ability Professional Network Clinical Research Associate
9 salaries
$95,663 per year
Leading CRO Company!! Clinical Research Associate
5 salaries
$99,504 per year
The Pursell Group Clinical Research Associate
7 salaries
$116,417 per year
PeaceHealth Clinical Research Associate
9 salaries
$35.36 per hour
new england physician recruitment center-boston Clinical Research Associate
9 salaries
$180,000 per year
MBA IT Consulting Services, Inc. Clinical Research Associate
7 salaries
$116,417 per year
Food Management Search Clinical Research Associate
7 salaries
$116,417 per year
Pharmaceutical Organization Clinical Research Associate
8 salaries
$246,884 per year
Texas Tech University Health Sciences Center of El Paso Clinical Research Associate
5 salaries
Clinical Research Associate Job available
$15.64 per hour
University of Wisconsin–Madison Clinical Research Associate
8 salaries
Clinical Research Associate Job available
$40,257 per year
Careers 2005 Clinical Research Associate
6 salaries
$104,485 per year
Taylee Staffing Clinical Research Associate
8 salaries
$102,227 per year
Rayco Technical Solutions, LLC Clinical Research Associate
6 salaries
$104,485 per year
Nishom Pharma Corp Clinical Research Associate
6 salaries
$70,000 per year
5 salaries
$57,250 per year
Real Life Sciences Clinical Research Associate
7 salaries
$117,035 per year
Inflamax Research Clinical Research Associate
6 salaries
$2,900 per month
Aptude Inc. Clinical Research Associate
7 salaries
$20.00 per hour
Virginia Commonwealth University Clinical Research Associate
8 salaries
Clinical Research Associate Job available
$36,729 per year
Scientific Search Clinical Research Associate
7 salaries
Clinical Research Associate Job available
$85,322 per year
ER Squared, Inc. Clinical Research Associate
6 salaries
$50,000 per year
Valesta Clinical Research Solutions Clinical Research Associate
7 salaries
$65,000 per year
On-Board Services Clinical Research Associate
5 salaries
$38.67 per hour
Military4Hire Clinical Research Associate
6 salaries
$104,485 per year
SSC Clinical Research Associate
8 salaries
$115,000 per year
Enterprise Search Associates Clinical Research Associate
6 salaries
$104,485 per year
The Fountain Group Clinical Research Associate
8 salaries
$135,000 per year
VetPharm, Inc. Clinical Research Associate
8 salaries
$47,500 per year
Pioneer Data Systems, Inc. Clinical Research Associate
7 salaries
Clinical Research Associate Job available
$50.00 per hour
The University of Michigan Clinical Research Associate
6 salaries
Clinical Research Associate Job available
$60,183 per year
North Peak Recruiting Clinical Research Associate
6 salaries
$104,485 per year
MedicusTek USA, Inc Clinical Research Associate
7 salaries
$42,000 per year
Genesis Global Management Corporation Clinical Research Associate
7 salaries
$105,971 per year
Quality Clincial Research Clinical Research Associate
5 salaries
$28,802 per year
The Job Jobber Clinical Research Associate
7 salaries
$88,043 per year
IMARC Research, Inc. Clinical Research Associate
5 salaries
$15.52 per hour
PHAIDON INTERNATIONAL Clinical Research Associate
6 salaries
$109,198 per year
Experis Clinical Research Associate
7 salaries
$38.63 per hour
Sunrise Systems Clinical Research Associate
7 salaries
$29.69 per hour
Small Niche CRO! Clinical Research Associate
6 salaries
$88,364 per year
University of Toledo Clinical Research Associate
5 salaries
$66,079 per year
Resource Employment Solutions Clinical Research Associate
6 salaries
$24.04 per hour
RELODE Clinical Research Associate
6 salaries
$5,000 per month
Painter & Associates Personnel Clinical Research Associate
6 salaries
$104,485 per year
Provident Research Inc Clinical Research Associate
6 salaries
$113,374 per year
RBW Consulting Solutions Ltd Clinical Research Associate
5 salaries
$109,280 per year
ParkPower Corporation Clinical Research Associate
5 salaries
$120,496 per year
Acara Solutions Clinical Research Associate
5 salaries
$19.80 per hour
Essentia Health Clinical Research Associate
5 salaries
Clinical Research Associate Job available
$16.73 per hour
New York State Psychiatry Institute Clinical Research Associate
5 salaries
Clinical Research Associate Job available
$45,068 per year
BRIDGEWAY COMMERCE GROUP Clinical Research Associate
5 salaries
$120,496 per year
NuWest Group Clinical Research Associate
5 salaries
$16.43 per hour
Pharmaceutical Clients Clinical Research Associate
5 salaries
$30.00 per hour
Byrnes and Rupkey, Inc. Clinical Research Associate
5 salaries
$120,496 per year
Cap & Sol Clinical Research Associate
5 salaries
$50.00 per hour
RCTS, Inc Clinical Research Associate
5 salaries
$13.15 per hour
All US Jobs Clinical Research Associate
5 salaries
$120,000 per year
The DAVIS Companies Clinical Research Associate
5 salaries
$25.00 per hour
JGB BioPharma Consulting Inc. Clinical Research Associate
5 salaries
Clinical Research Associate Job available
$112,945 per year
Advanced Technology Solutions Clinical Research Associate
5 salaries
Clinical Research Associate Job available
$43.55 per hour
Worldwide Clinical Trials Holdings, Inc. Clinical Research Associate
5 salaries
$109,545 per year
Private Practice Leadership, LLC Clinical Research Associate
5 salaries
$15.71 per hour
Team1Medical Clinical Research Associate
5 salaries
$33,786 per year
ZEISS Group Clinical Research Associate
5 salaries
$48.00 per hour
Worldwide Placement Limited Clinical Research Associate
5 salaries
$90,000 per year
Pharmaceutical Research Associates, Inc. Clinical Research Associate
5 salaries
$76,530 per year
Healthcare Recruiters International Clinical Research Associate
5 salaries
$62,430 per year
Bridgeway Professionals Clinical Research Associate
5 salaries
$120,496 per year
i-Pharm Consulting Clinical Research Associate
5 salaries
Clinical Research Associate Job available
$94,767 per year
Collaborative Clinical Research Associate
5 salaries
$39.65 per hour
The Veritas Healthcare Solutions LLC Clinical Research Associate
5 salaries
$78,850 per year
Louis Stokes Cleveland VA Medical Center Clinical Research Associate
5 salaries
$43,399 per year
Piper Enterprise Solutions Clinical Research Associate
5 salaries
$111,929 per year
Groupware Solutions Clinical Research Associate - CRA Course
5 salaries
$30.00 per hour
Take courses from CCRPS and learn more on how to become a clinical research professional.
Discover more from Clinical Research Training | Certified Clinical Research Professionals Course
Clinical Research Career Salaries (CRA, CTA, CRC, ect)
CCRP Course Provides Certification to work in the following roles
Senior Clinical Research Associate (CRA) 200 profiles
$101,978 $74K-$121K
Clinical Research Associate (CRA) 198 profiles
$67,532 $44K-$106K
Clinical Trial Manager 56 profiles
$102,283 $69K-$139K
Clinical Project Manager40 profiles
$111,006 $73K-$136K
Clinical Operations Manager 7 profiles
$116,859 $108K-$125K
Clinical Research Manager 6 profiles
$108,250 $98K-$119K
Associate Clinical Research Director 5 profiles
$136,950 $116K-$148K
The tuition fee is $1,795 ($18 per module) is offered over a 4-month payment plan in this link. The online training can be completed within 1-4 months time and can start within 24 hours of tuition payment.
Are you looking to work in the clinical research field? CCRP Courses provides certification to work in the following roles:
Senior Clinical Research Associate (CRA)
$101,978 on average, from $74K-$121K.
Enhance your expertise as a Senior CRA
with our CRA Certification Course.
Clinical Research Associate (CRA)
$67,532 on average, from $44K-$106K.
Start your career with our CRA Certification Course.
Clinical Research Coordinator (CRC)
$50,451 on average, from $38K-$68K.
Learn more about becoming a CRC with our
Clinical Research Coordinator Course.
Clinical Trial Assistant (CTA)
$45,412 on average, from $31K-$66K.
Explore how to become a CTA with our
Clinical Trials Assistant Training.
$102,283 on average, from $69K-$139K.
Advance your career with our Advanced
Clinical Research Project Manager Certification.
$111,006 on average, from $73K-$136K.
Further your skills with our Advanced Clinical
Research Project Manager Certification.
$116,859 on average, from $108K-$125K.
Deepen your expertise with our Advanced
Clinical Research Project Manager Certification.
$108,250 on average, from $98K-$119K.
Our Clinical Research Coordinator Course
can help you excel in this role.
Associate Clinical Research Director
$136,950 on average, from $116K-$148K.
Develop your leadership skills with our Advanced
Principal Investigator Physician Certification.
The tuition fee is $1,795 ($18 per module) is offered over a 4-month payment plan in this link. The online training can be completed within 1-4 months time and can start within 24 hours of tuition payment. Our courses are ACCRE accredited and curated by field professionals that know what they are doing. Click below to learn more about clinical research positions.
Take courses from CCRPS and learn more on how to become a clinical research professional.
Discover more from Clinical Research Training | Certified Clinical Research Professionals Course
CCRPS Clinical Research Certificate Program Overview
This program enables you to master practical aspects of clinical trial conduct and management. For more info read our blog.
The First Step to Clinical Research Certificate Program
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CCRP CRRA Certified Clinical Researcher Associate
This program requires only a medical sciences education background such as FMGs, BSNs, and Bachelors graduates. Clinical Research Associate Training Course is a 110 module course led by Senior CRA and Physician of 25 Years, Dr.Kamal. This course provides the training, experience, interviewing, letter of references, and connections you need to get a job supervising clinical research efforts. We offer clinical research associate training and placement for nurses, science bachelor graduates, and international medical graduates.
For those interested in expanding their knowledge and skills, consider enrolling in the CRA or the Advanced Clinical Research Project Manager Certification courses for further specialization.
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SCDM CCDM Certified Clinical Data Manager
Eligibility Requirements
APPLICANTS FOR THE CERTIFIED CLINICAL DATA MANAGER (CCDM™) PROGRAM MUST MEET ONE OF THE FOLLOWING CRITERIA
Bachelor’s degree or higher and minimum two years full-time CDM experience
Associate’s degree and minimum three years full-time CDM experience
Four or more years full-time CDM experience
Part-time work experience equal to or surpassing full-time equivalent in criteria above
ACRP CCRA Certified Clinical Research Associate
The CCRA® eligibility criteria define the minimum experience required before a CRA can apply for the program. It is important to compare the CRA eligibility criteria with your career and educational experiences to self-determine your eligibility before submitting an application and payment. All applications must undergo a formal review process to determine an applicant’s eligibility to sit for the exam.
CRA Certification Eligibility Requirements
In order to be deemed eligible to take the CCRA® exam, applicants for the CCRA® credential must be able to provide evidence through a job description, detailed CV, or other documentation that they:
Work independently of the investigative staff conducting the research at the site or institution. This means they do not report to the PI or site manager and that they do not have the ability to change or manipulate data, and;
Work on behalf of the sponsor. This means that they are contracted by the “sponsor” to perform an independent monitoring function. The “sponsor” can be a pharmaceutical or device company, a granting agency, a university department, a physician, etc., and;
Perform all of the CCRA® essential duties as detailed below for a required minimum number of hours. Hours performing the CRA essential duties can include hoursdocumented up to the date of the exam and/or through previous employment. The required number of hours is dependent upon one’s educational background.
The CRA Certification Handbook has complete information on eligibility requirements.
ACRP CCRC Certified Clinical Research Coordinator
CRC Certification Eligibility Requirements
In order to be deemed Eligible to take the CCRC® exam, applicants for the CCRC® credential must be able to provide evidence through a job description, detailed CV or other documentation that they:
Perform all of the CRC essential duties as detailed below for a required minimum number of hours.
Hours performing the CRC essential duties can include hours documented up to the date of the exam and/or through previous employment. The required number of hours is dependent upon one’s educational background.
For those pursuing a career as a Clinical Research Coordinator, the Clinical Research Coordinator course provides essential training and certification.
SoCRA CCRP Certified Clinical Research Professional
The applicant must be working with Good Clinical Practice (GCP) guidelines under IRB/IEC/REB-approved (or specifically exempted) protocols.
The applicant must meet one of the following Eligibility Criteria noted below. Please note that most candidates will be eligible under Category 1.
For purposes of eligibility, please view SOCRA's definition of a Clinical Research Professional.
If you have a question about Candidate Eligibility please email SOCRA at certification@socra.org
Consider enhancing your understanding of GCP with the ICH-GCP course.
Category 1
Applicant must have (and be able to document) ALL of the following qualifications:
Have two years of experience as a full-time Clinical Research Professional (or have 3,500 hours part-time) during the last five years
Please note: If you have completed two (2) years of full-time employment as a clinical research professional in the past five years, you will NOT need to provide supporting documentation for your educational experience.
Category 2
Applicant must have (and be able to document) ALL of the following qualifications:
Hold a degree in "Clinical Research" from an Associate, Undergraduate, or Graduate Degree Program AND
Have completed a minimum of one year of full-time experience (or 1,750 hours part-time) during the past two years as a Clinical Research Professional
Category 3
Applicant must have (and be able to document) ALL of the following qualifications:
Hold an Undergraduate or Graduate Certificate in “Clinical Research” with a curriculum of no less than 12 semester (credit) hours or totaling a minimum of 144 credit hours from an academic institution of higher learning (community college, college or university) AND
Hold an Associate’s or Bachelor’s Degree in a science, health science, pharmacy or related field AND
Have completed a minimum of one year of full-time experience (or 1750 hours part-time) during the past two years as a Clinical Research Professional.
ACRP CCTI Certified ClinicPrincipal Investigator
The CPI® eligibility criteria define the minimum experience required before a PI can apply for the program. It is important to compare the CPI® eligibility criteria with your experience to self-determine your eligibility before submitting an application and payment. All applications must undergo a formal review process to determine an applicant’s eligibility to sit for the exam.
PI Certification Eligibility Requirements
In order to be deemed eligible to take the CPI® exam, applicants for the CPI® credential must be able to provide evidence through a job description, detailed CV or other documentation that they:
Have a doctorate level degree and;
Have proof of employment as a PI during at least two (2) of the most recent five (5) years and;
Perform all of the essential duties as detailed below.
The PI Certification Handbook has complete employment definitions.
Update: The CPI Exam is the first exam being offered to all investigators with a doctoral-level degree. A license to practice medicine is no longer required.
NAIM CIM Certified IRB Manager
To qualify for the Certified IRB Manager Examination, you must meet the following
requirements:
• Applicants must have a Bachelor’s Degree and 2 years of relevant IRB
Management experience within the last 5 years.
OR
• An Associates Degree from a two year college or technical school and 2 years
of relevant IRB Management experience within the last 5 years.
CCIP CIP Certified IRB Professional
Eligibility Requirements
This certification program is for individuals whose primary job responsibilities include substantial participation in overseeing, administering or performing the daily activities of an IRB as part of a HRPP. Individuals involved in IRB activities who meet the following eligibility requirements are eligible to take the examination:
A Bachelor's degree plus two years of relevant HRPP experience, completed on or before the first day of your chosen testing period (see front cover)
or
Three years of relevant HRPP experience, completed on or before the first day of your chosen testing period
or
Current certification as a CIP
RACC CRA Certified Research Administrator
Bachelor’s Degree and three (3) years of professional experience in research or sponsored programs administration either in a sponsoring or recipient organization or the equivalent in a self-funded organization;
OR
An Associate’s Degree and five (5) years of professional experience in research or sponsored programs administration either in a sponsoring or recipient organization or the equivalent in a self-funded organization;
OR
No degree and six (6) years of professional experience in research or sponsored programs administration either in a sponsoring or recipient organization or the equivalent in a self-funded organization. *
MAGI CRCP Certified Research Contract Professional
People often ask how to prepare for the exam. Two years of experience with a variety of negotiation partners may be sufficient to pass the exam. A careful reading of MAGI's Model CTA, Clinical Trial Agreement Handbook (Original), and Model CDA is helpful. There are numerous relevant articles in the Journal of Clinical Research Best Practices. Attending MAGI's Clinical Research Conference is good preparation, provided you attend sessions and workshops that address relevant topics where you need more knowledge. Sample questions, study guides, or other study materials are not available. However, imagine an exam for professional chefs. One question might be, "Describe the process of making an omelette." Another might be, "List five spices used in Chinese cuisine." Another might be, "What are the pros and cons of gas vs. electric stoves?"
RAPS RAC Regulatory Affairs Certification
The RAC is the only credential for regulatory professionals in the healthcare product sector. The RAC demonstrates to employers, clients and colleagues essential knowledge, critical thinking abilities and a commitment to continuing professional development. It is designed for working regulatory professionals, with at least three to five years of regulatory experience. There are six different RAC exams. The US, EU and Canada exams test regional regulations and involvement with regulatory bodies. The global exam focuses on international standards and guidelines. The devices and drugs exams have a global focus yet aligns to a specific sector of regulation knowledge. All six exams test for regulatory knowledge, critical thinking and analysis throughout the lifecycle of a product.
SQA RQAP Registered Quality Assurance Professional
The Society of Quality Assurance is proud to offer the professional credential Registered Quality Assurance Professional (RQAP) for professionals working in Good Laboratory Practices as well as for professionals working in Good Clinical Practices. Registration is a recognized standard of experience and knowledge throughout the QA industry, in the US and around the world.
What the credential demonstrates
Proof of your knowledge of the regulations/guidelines and how they are applied
Commitment to a high quality standard in the QA industry
Personal professional growth and achievement
How it Works
Professionals must pass an examination in either Good Laboratory Practices or Good Clinical Practices to receive the RQAP credential.
Registered professionals must re-register every three years by submitting documentation of ongoing professional activities. These activities include, but are not limited to:
Attending the SQA Annual Meeting and/or Quality College
Attending events of SQA Regional Chapters
Attending events of relevant professional associations/societies, e.g. JSQA, RQA, RAPS, DIA, ACS, ACRP, NAICC, AALAS, etc. (See our MOU Organizations and Liaison Organizations.)
Completing courses in the SQA Online Learning Center
Attending SQA webinars or webinars offered by relevant professional organizations
Studying the SQA Annual Meeting Online Library
Participating in the SQA Mentoring Program
Writing test items for an RQAP exam
Take courses from CCRPS and learn more on how to become a clinical research professional.
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From The Course Creator: CRA Clinical Research Certification & Training
CRAs can expect to make between $75-90k/year within their first year. CRAs who are physicians from foreign countries are considered MDs in this position. CRAs who are nurses which transitioned are treated remarkably well among the hospitals they visit or monitor. As a supervisor of clinical trials, this also paves ways to enter higher-level administrative and leadership roles in medical centers, institutions, and pharmaceutical companies.
Clinical research associates are currently the highest paid upper-level medical professionals in the pharmaceutical and medical industry, second only to physicians. Many remote and traveling (expenses-covered) jobs are available for CRA positions for those who have a background or certification training. If you're looking to further enhance your qualifications, consider our Clinical Research Coordinator course or our comprehensive CRA training.
The obvious difficulty in searching for these positions is getting selected and interviewed without experience. CCRP Course works directly with:
International Medical Graduates (MBBS, FMG, IMGs)
MDs without residence
Bachelor’s of science or healthcare-related fields
Bachelor’s of nursing and nurses
Master’s of science graduates
CCRPS’ courses strives for you to achieve the knowledge, certification, and resume experience needed to be selected and hired by pharmaceutical companies. For those involved in monitoring, consider our Medical Monitor Certification to boost your credentials.
CRAs can expect to make between $75-90k/year within their first year. CRAs who are physicians from foreign countries are considered MDs in this position. CRAs who are transitioned nurses are treated remarkably well among the hospitals they visit or monitor. This role also offers pathways into higher-level administrative and leadership roles in medical centers, institutions, and pharmaceutical companies, which can be further supported by our Advanced Principal Investigator Physician Certification and Advanced Clinical Research Project Manager Certification.
As a supervisor of clinical trials, this position also paves ways to enter higher-level administrative and leadership roles in medical centers, institutions, and pharmaceutical companies.
Courses for Quality CRA Training Modules per Course
1. ICH GCP Training 15
2. Quality Monitoring 45
3. Regulatory Training 15
4. Audit and Inspections 6
5. Writing Professional Monitoring Reports 16
-Developing Follow Up Reports
6. Subject Recruitment Retention and Compliance 5
7. Misconduct and Fraud 2
8. Competency Testing of CRA’s 6
………… Total 110 Modules
Training certification will be provided at the end of the course. This can be listed on your resume as an educational experience as well as a volunteer experience for the amount of time it takes you to complete the course.
The tuition fee is $1,795 ($18 per module) is offered over a 4-month payment plan in this link.
The online training can be completed within 1-4 months time and can start within 24 hours of tuition payment.
After module completion we begin your recruiter-interaction training by providing the following:
1. Interview Prep (3 interview rounds training)
2. Resume experience of training
3. Recruiter based references
4. Multiple employee references
5. LOR’s
Having been a Senior CRA for 15 years, my job is to ensure that entering and succeeding this field is easier for our students. If you are interested in this field, below are some CRA articles you may find useful.
Take courses from CCRPS and learn more on how to become a clinical research professional.
Discover more from Clinical Research Training | Certified Clinical Research Professionals Course
How to Become a CRA in Canada: Clinical Research Associate Certification
How to Become a CRA in Canada
How to Get A Clinical Research Associate Certificate Online in Canada
CCRPS offers Canadian CRA certification for students living and working in Canada. A CRA certification in Canada provides students with additional knowledge of resources and guidelines in order to work in clinical research.
Our certification specifically state and prove that you have reviewed Canadian guidelines in clinical research and meet the competencies required for all clinical research associates.While our certificate is accredited by the ACCRE, 4 other organisations, and shows employers you have the working knowledge to act as a CRA; the CRAC credentialing exam will help further establish your professionalism. If you already have experience as a clinical research associate, you can use this course to prepare and sit for the CRAC examination.
In order to become a certified Canadian CRA, you must take the CRAC credentialing examination. To sit for the examination, you must fulfill one of these requirements:
2 years of clinical research expereience within the last 5 years
3,500 hrs of part time experience with at least 1 year of Canadian experience within the last 5 years
A post-graduate certificate in clinical research and at least 1 years’ experience over the past 2 years in clinical research. You must have at least 1 year of Canadian experience.
2. Clinical Research Associate Canada (CRAC) Membership
While CCRPS membership is free, you still benefit from obtaining CRAC membership even if you do not have enough experience to sit for the CRAC credentialing exam. Membership can create networking and job opportunities, as well as provide insight into the field. All interested professionals should become a Member of the Official Canadian CRA Association and list this involvement on their CV and cover letter.
3. CCRPS Canadian CRA Certification (CCRAC) for Resume Building
As we teach nearly 30 Canadian students each quarter, our Canadian Clinical Research Associate Certification will allow students to strengthen their application and resume, specifically towards Canadian guidelines and policies.
4. Landing A Entry Level Clinical Research Associate Job in Canada
Unfortunately, many professionals have trouble securing a job in order to get experience and take the CRAC exam. Our certification, specifically created for Canadian CRAs, provides entry-level science professionals with all the resources they need to be a working CRA in Canada. Our online exam can be taken at any time, if you enroll or demo our course.
5. Clinical Research Associate Programs in Canada
In addition to providing 130 modules, our CRA certification exam is priced affordably and the same as our American students. Students can gain valuable work experience by applying to be one of our CCRPS Clinical Research Education Fellows for a 1 month remote internship to develop and strengthen your resume.
6. Salary of Canadian Clinical Research Associate
Payscale Canadian CRA Salary
Payscale Canadian Pay Difference CRA
Clinical Research Certification Specifically for Canadian CRAs
CCRPS offers one of the only online certifications specifically designed for entry-level and mid-level professionals in clinical research associate knowledge. We prepare you to understand and apply all skills required to secure a job in clinical research.
Canadian Clinical Research Associate Certificate Course Preview
Want to Learn More About Clinical Research?
Take courses from CCRPS and learn more on how to become a clinical research professional.
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Discover more from Clinical Research Training | Certified Clinical Research Professionals Course