begin a Career in Clinical Research

How you ever thought that there’s a perfect job out there for you, but you just haven’t found it yet? If you are motivated, informed, and interested in a science and medical career, you might have just found your answer. Many clinical research professionals say this is the golden ticket to a great career in the science field.  

Why Clinical Research as a Career

The clinical research industry is a highly lucrative and expanding field. The global clinical trials market has been estimated at $46.8 billion in 2019.

As the push for new vaccines and therapeutics continues to get stronger, the field is expected to grow even more in value. Experts predict that the global market will hit $69.9 billion by 2027. The future in clinical research is bright, and it is one that you will want to be a part of.

Contrary to popular belief, working in clinical research doesn’t have to mean you have to stay in a lab. There are demands and opportunities for every skill set, if you know how to find them. Below, I have put together an in-depth guide on why you should get into clinical research.

Working in Clinical Research

1. You like a job that’s flexible

Don’t like working in a cubical? How about heading to the airport every morning instead? If you like a job that keeps you moving, then becoming a Clinical Research Associate (CRA) and working in clinical trials might be the right move for you. Learn more about becoming a CRA with this CRA Certification Course.

CRAs, contrary to what most people believe, don’t collect data or interact with patients. A CRA’s day-to-day job is to travel between different research sites and verify data transcription (i.e., data management). CRAs can also become part of the project management as a clinical trial manager of an entire trial.

They are also called “monitors” and a part of "regulatory affairs", because it is also their job and clinical experience to ensure that every site is following proper compliance and protocols.

There are two types of CRAs: home base or in-house. Home base CRAs work remotely. That means they work and travel from home. Most CRAs work for contract research organizations who are hired by sponsors to conduct their multi-site trials.

If you get tired of working home base, you can become an in-house CRA. In-house CRAs stay in one site and work together with a home base CRA to keep each other updated with what is happening at their site.

1. You like working with people

Have you ever been told that you are a people person with great communication skills? If talking to someone about how you can change their health for the better sounds like something you’d enjoy, you should definitely look into becoming a Clinical Research Coordinator (CRC). Explore our Clinical Research Coordinator Course to get started.

CRCs are the backbones to every project. They conduct patient visits, input source documents into the electronic data capture (EDC), and ensure that every trial is following compliance. They are also responsible for handling regulatory documents and updating the Principal Investigator (PI) with trial results.

CRCs conduct a variety of tasks, all of which impact the progress and development of the trial. Every successful clinical trials team needs is a good CRC. So, if you have strong interpersonal skills and know how to stay organized, you will be an indispensable part of the team.

1. You are detail-oriented and tech-savvy

Are you a self-proclaimed techie? Perhaps you’ve dabbled in coding, pick up computer programs easily, and maybe even have a background in IT. Technology is the future. If you think you have a knack for organizing data, you should look into becoming a Clinical Trial Assistant (CTA). Check out our Clinical Trials Assistant Training to learn more.

CTAs, also known as Clinical Research Assistants, manage the Trial Master File (TMF). They file, archive, and maintain trial documents and study files. They are also responsible for closing inquiries from the CRA, as well as providing administrative support to the research team. Every important step in clinical research, pre-clinical research, study startup, site management, needs a dependable CTA.

While most jobs in clinical research require some understanding of technology, it is especially important for the CTA to know what they are doing when it comes to managing trial documents and study files. In addition, it is equally important that the CTA is organized and knows how to pay attention to detail.

Working in Clinical Trials

1. Means you like a good salary...with room for promotion

Though there are many career paths within clinical research, most people begin their career as CTAs or CRCs in entry-level positions. Depending on your skill set and what kind of experiences you can bring to the table, either position will help you get your feet through the door.

According to salary.com, a CTA’s average salary in 2020 is $63,000. They generally earn between a range of $54,300 and $73,000, and are provided with benefits such as healthcare and social security.

If being more hands-on in the research process appeals to you, you might be a good fit for a CRC. Similarly, CRCs are making an average of $63,117 in 2020. Most make between a range of $54,210 and $72,902, plus employee benefits.

While numbers tend to fluctuate between cities and states, there’s no denying that these are great salaries for an entry position. Since according to one of the largest global job recruitment sites, Glassdoor, the average base salary in America is $40,000. Starting with an annual salary of $60,000 is considered uncommon and on the high end of the spectrum.

After one to two years of experience on the job, most companies provide CTAs and CRCs opportunities for professional development and promotion. Many become Clinical Research Associates, or CRAs. Indeed reports that the average salary of a CRA with one to two years of experience is $72,358. After building at least 6 years experience, a seasoned CRA should expect to earn $110,102 a year. If you would like to make more money, you can consider becoming an individual contractor CRAs. They can earn up to $300,000 in a year.

1. You are a science professional wanting to change careers and don’t want to go back to school

In clinical research, experience is often valued over degrees. Rather than what you didn’t study in college, hiring managers are more interested in what you have done in the past and how they can integrate you into their company.

This includes getting certified through clinical research courses, but more so what you learn from the courses you take. CCRPS offers the most in-depth CRA and CRC training so that there's tons to talk about during the interview and a working bank of knowledge during the first few months of the job. Explore more specialized certifications like ICH-GCP, Advanced Clinical Research Project Manager Certification, and Advanced Principal Investigator Physician Certification to further enhance your qualifications.

While graduate programs can help point you in the right direction, you don’t need a master’s degree to succeed in clinical research. In fact, certain positions don’t even require a bachelor’s or associate’s degree; they have certification in clinical research.

Applying to CRC and CTA positions are one of the most common segways into higher positions in clinical research. CRCs don’t need a bachelor’s or associate’s degree to get their foot in the door. While both CTA and CRA positions require a bachelor’s degree, they don’t have to be in the life sciences.

One of the best ways to gain experience and stand out from the crowd is to have on-site experience. If you need advice on how, Dan Sfera, the CEO of DSCS CRO Clinical Research Services, recommends getting started by interning or volunteering at clinics and research sites to build connections and experience.

Sometimes, the easiest way to get involved is to offer services like patient recruitment and social media management in exchange for opportunities to build your CV. By appealing to a site’s needs, this will help you get your foot in the door and build the connections and resume you need.

Another great way of adding experience to your resume is by training throughcertification courses. When employers see that you have taken the time and effort to understand how to be the best in their field, they are more far likely to hire you. At CCRPS.org, we offer seven courses and certification trainings to give you an advantage. Most of our students are hired within the first month of taking the course. We are accredited by the Accreditation Council For Clinical Research Education (ACCRE) and Joint Commission by the AMA, ANCC, and various other organizations to provide 17.5 CME credits through our CRA Certification and CRC Certification.

6. You are switching careers

Switching career fields can be nerve wracking. However, it is also an opportunity for you to be a unique candidate. Whether you come from a closely-related background, like medicine or nursing, or something completely different, there are ways you can advocate for yourself in front of employers.

If you already have a background in medicine (nonclinical doctor, unmatched MD), your knowledge of healthcare and your passion for patient health will make for a smooth translation into clinical research. In addition, your RN or MD degrees will help you gain a competitive edge and allow you to climb higher positions, such as the PI, who is the primary researcher of an operation. 

On the other hand, if you come from a less relevant field but feel passionate, you can still leverage yourself to be exactly what the clinical research field needs. For example, if you are a teacher, your communication and interpersonal skills will be your keys to success. If you are a lawyer, your ability to draft and read papers will far surpass the average candidate.

If you studied mathematics, you are a skilled problem solver. If you are a translator, your language skills are valuable and will help you get into roles that require it. In short, whatever skills helped you succeed in your previous positions, you can bring it with you to clinical research. 

7. You want to make a difference in disease outcomes and patient care

There are two types of people in the world: ones who accept the world as it is, and ones who strive to change it. In the last 50 years, science and medicine have gone through a series of drastic changes. However, anyone who works behind the scenes will tell you that medical breakthroughs are not miracles. Clinical research is the culmination of human effort and intelligence.

The fruits and labor of the ever-expanding industry are proof that if enough people care about the world, then they can change it. While there are many good reasons to work in clinical research, if you want the privilege to enrich the lives of others, there is a place for you in this field.

If you want to take a sneak peak at employers and opportunities near you, jobs sites like Indeed are a great resource. 

Here are links for aspiring CRAs, for CRCs, and for CTAs. (Note: CTAs are often referred to Clinical Research Assistants, not to be confused for Clinical Research Associates)

7 Steps to Launching Your Career as a Clinical Research Coordinator

The prospect of a career in clinical research can be exciting, especially for those with a passion for science, medicine, and helping others. A Clinical Research Coordinator (CRC) plays a vital role in this field, ensuring research is conducted ethically and efficiently. If this sounds like the path for you, here are 7 essential steps to becoming a successful CRC:

1. Earn a Relevant Degree:

   A bachelor's degree in a science-related field like biology, chemistry, or healthcare administration is typically required (National Institutes of Health .gov). Some employers may prefer a master's degree for more specialized roles (National Institutes of Health.gov). Consider exploring the Clinical Research Coordinator course for targeted training in this role.

2. Gain Hands-on Experience:

   Internships or entry-level positions in clinical research settings offer invaluable experience (Association of Clinical Research Professionals (ACRP)). This practical exposure strengthens your resume and provides real-world knowledge for future CRC roles. Gain further insights through the Clinical Trials Assistant Training course.

3. Consider Certification:

   While not always mandatory, CRC certification enhances your credentials and marketability. Programs like those offered by the ACRP validate your expertise and set you apart from other candidates. Expand your certification options with the CRA course and the ICH-GCP course.

4. Develop Core Skills:

   Crucial skills for CRCs include: attention to detail, organization, critical thinking, and effective communication. A strong understanding of research regulations and ethics is also crucial. Enhance these skills through the Advanced Clinical Research Project Manager Certification.

5. Build Your Network:

   Attend industry events, conferences, and seminars to connect with professionals. Networking opens doors to opportunities, mentorship, and valuable industry insights. Consider further specialization with the Advanced Principal Investigator Physician Certification.

6. Apply for CRC Positions:

   With your qualifications, certifications, and experience in place, actively seek CRC positions. Tailor your resume to highlight relevant skills and experiences, and craft a compelling cover letter showcasing your passion for research. Research the organization and demonstrate your knowledge during interviews.

7. Embrace Continuous Learning:

   The field of clinical research is constantly evolving. Stay informed about industry trends, participate in continuing education, and pursue professional development opportunities to stay ahead in your CRC career. The Pharmacovigilance Certification and the Medical Monitor Certification can be instrumental in your continuous learning journey.

References:

• National Institutes of Health (.gov): https://toolkit.ncats.nih.gov/glossary/clinical-research-coordinator/

• Association of Clinical Research Professionals (ACRP): https://acrpnet.org/

• Society for Clinical Research Associates (SCRA): https://www.scra.org/

How To Get Clinical Coordinator Certification?

The clinical coordinator or CRC is also known as the clinical trial manager. They play an essential role in the studies of medicine of all types. They work typically under the personal investigator who has a charge of managing and conducting the clinical trial at a higher level. CRC's job is to facilitate, support, and to organize the daily trial activities of the clinical. Getting a clinical coordinator certification online will take a lengthy procedure. There are some kind of the CRC at very different phases of various educational achievements. Let's look at the steps which you will need to get the clinical coordinator certification.

Step 1: Must Be Graduate From High School (4 Years)

For preparing for the clinical coordinator certification, you must begin with high school courses like biology, chemistry, and physics, also with the maths and communications. This will found your form of the foundation which will be pursued for the college studies, which also be the four-year studies.

Step 2: - Obtain A Bachelor Degree Of 4 Years

When perusing the universities and the colleges, you must focus on the courses which offer you a bachelor's degree in health sciences in terms of clinical research administration. The students should dedicate them all the things to obtain this degree and must concentrate only on this for pursuing the degree full time. These programs generally provide the clinical research professional with the tools which they will need to do the developing their medical sciences and conducting their trials and also studies. Both on the campus and the online programs on the clinical administrations focus on clinical research for placing to protect the human subjects.

The bachelor's degree can give you an entry-level position in the clinical organization or any institution. It will also help you with the existing clinicians with the advance, which is in the current jobs. The students who wish to pursue more opportunities in terms of responsibility and also the salary might also be interested in specialized training such as the Clinical Trials Assistant Training or the Advanced Clinical Research Project Manager Certification.

Step 3: - Gain Some Professional Experience

In this step, you will need to gain some experience in the field. You will have to work in clinical research with full-time research. This is the requirements for qualifying the national clinical coordinator certification. For those looking to expand their knowledge in specific areas, consider the Advanced Principal Investigator Physician Certification or Medical Monitor Certification.

Step 4: -Obtain Online

In this step, the students can get an online graduate certificate in the clinical researcher, which can be of 1 year. This will help the students to grow some knowledge around the medical world. It will help the students for getting the clinical coordinator certification. Here you can explore many types of concepts of science and designing research, data management, professionalism, and leadership. This degree will offer you strong knowledge in clinical examination, ethical research and will also provide you the experience of the medical management skill related to drugs and other trials of therapeutic. For those interested in further certification, the ICH-GCP course is also available.

Step 5: - Online Master Of Science In Clinical Research Management

This online Master of Science course is done for increasing the salary purpose of the clinical research. This is a two years course. This course includes the clinical study of coordinators and as well as the data manager of the clinical, research assistants of the social science, and also about the clinical tech laboratories. Here you can explore many types of concepts of science and designing research, data management, professionalism, and leadership. After this course, the students will get some handsome salary and also be eligible for higher-grade jobs in clinical research. This will benefit you is pursuing the clinical coordinator certification. Those interested in Pharmacovigilance may consider the Pharmacovigilance Certification to enhance their expertise in this critical area.

Get The Certification

Now it's the time to hold the accreditation of your hard work, and it determines your success. There are some categories of certifications that will help you to understand which category you fall in.

The COVID-19 crisis has created a new normal in the workplace. Many companies have required their employees to work remotely as much as possible, and the clinical research field is no different. In this unprecedented time, the FDA has encouraged the use of technology, telehealth, and remote drug deliveries for conducting clinical trials. For many clinical research professionals, the shift to remote work can be challenging and difficult to navigate. However, experts believe that virtual clinical trials are going to be a huge part of the field’s future. To effectively manage these trials, consider the Advanced Clinical Research Project Manager Certification. This article has compiled some of the best tips and tricks to help you plan a productive and fulfilling workday at home.

Check Out Company Guidelines

Working in a pandemic is a special circumstance that deserves special considerations from employers. What a lot of people forget is that most companies have created HR guidelines for employees working during a time of crisis. Reviewing these guidelines can help you understand your company’s remote work policies, as well as procedures and expectations. For those looking to further understand and comply with regulatory standards, consider exploring the ICH-GCP course to deepen your knowledge on international guidelines. Additionally, the role of Pharmacovigilance Certification is crucial in ensuring drug safety, which is paramount during such trials.

Enhancing Team Coordination

Effective communication is key in remote work settings, especially when coordinating clinical trials. Clinical Trials Assistants play a vital role in this, and gaining specialized skills through the Clinical Trials Assistant Training can enhance your ability to manage projects efficiently. For Clinical Research Associates (CRAs), who ensure the smooth execution of these trials, the CRA certification can provide the necessary training to adapt to the evolving landscape.

Special Roles in Clinical Research

For advanced positions such as Medical Monitors and Principal Investigators, specific certifications like the Medical Monitor Certification and the Advanced Principal Investigator Physician Certification are essential. These certifications prepare you for high-level oversight and critical decision-making roles necessary for the success of remote clinical trials.

Set physical and social boundaries

One of the chief complaints of working from home is being unable to focus. It is easy to get distracted when you are a few steps from the TV, or you are sharing the space with other people. To have a distraction-free workday, it is important to create a designated workspace that you feel comfortable working in. This way, as soon as you enter the room, your brain is ready to concentrate on the right thing. 

In addition, although it is important to socialize, set boundaries with those around you to make sure that you leave the socializing to after work is over. 

Get into a Routine

Even though you are working from home, it can be very helpful to a structured schedule. When creating a work routine, it is not only important to determine when you should start working, it is also important to determine when you should stop. This helps prevent burnout and allows you to focus on other important things in your life. 

Get the Right Tech

When you’re in clinical research, having reliable technology is vital to many positions. For example, it is important that your computer can run the programs and softwares you need for your job. Otherwise, you might have to consider getting an upgrade before going remote. Additionally, it is important that you understand how to use virtual communication programs like Zoom, so you can connect regularly and effectively with your boss and colleagues.

Over Communicate

Out of all of the tips discussed in the article, this one is the one that most experts agree on. As you begin working remotely, you will notice very quickly that it is harder and more important than ever to connect with your colleagues and managers. It is not only helpful to update your colleagues and bosses more frequently, it is also important to keep up social habits you had before the pandemic. If you always talked to a particular colleague before the weekly meeting, try giving them a call before the same virtual meeting. This way, you’ll be able to maintain your old routine and keep up with your office even when you’re working from home. 
Since the pandemic has drastically changed the way we work, here are some new ways to elevate your workday at home. As discussed in our other article, clinical research is developing a new perspective that generates new opportunities and to change the field. Virtual clinical trials (VCTs) are going to stay in the field, and the technical and self knowledge you gain working during this time will serve you well in future clinical research projects. If you want to learn more about the clinical research profession, please check out our specialized training programs and articles below to learn more about the clinical research job scene.

Learn more Work From Home Tips by Katie Holmes

Roles And Duties Of Clinical Trial Coordinator

A clinical research coordinator or a clinical trial coordinator (CRC) is in charge of managing clinical research at clinical research sites as per the protocol, ICH- GCP, and some other regulatory needs. The function of a study administrator in clinical research is very crucial. All the sites of a clinical trial have one or more study organizers relying on the workload at the research site. The clinical trial coordinator certification is required in such research sites. 

The site-level clinical trial can roughly be classified into three stages:

1. Before starting the clinical trial: In this stage, the study organizer has to collect and finish questionnaires collected from different sponsors and various CROs. Clinical research coordinators also have to collect data from the principal investigator and dispatch them back to the people who had communicated to this site for the study. The sponsors choose locations based on responses submitted in the feasibility questionnaire and finally direct pre-site assortment visits to finalize the plots taking part in the conduct. The sites conducting the research work must have clinical trial coordinator certification to carry on with investigator meetings. These investigator meetings are held at the international level or national level. Before beginning with the trial, the clinical research conductors are usually busy in the submission of various documents to the ethics committee. Besides, subject diaries, investigators CVs, clinical research agreement, signature page of protocol, clinical trial coordinator certification, indemnification letter, insurance certificate, blank CRF's, various study logs, etc. are also required to be submitted. A clinical study organizer plays a vital role in these processes. The site-level can then initiate the clinical trial after getting permission from the ethics committee.  

2. Conduct during the clinical trial: The clinical research conductor must have a good knowledge regarding the study protocol and should have a good idea of exclusion and inclusion criteria by the time clinical research is conducted. The study coordinator needs to have consent informed from the subject represented to do by the Principal Investigators. The study administrators need to collect subject pre-medical records, clinical trial coordinator certification, and according to investigation protocol, the person will have to manage issues programmed visits. Before visiting the item randomly, the clinical research coordinator must check exclusion and inclusion criteria, and after that, the entitled subjects are to be enrolled. After completing all the procedures of the visit, coordinators need to present information in the form of a case report. The clinical study coordinator should keep all relevant data and files up to date. In the next step, the CRC has to calculate the study drug accountability. Interactive web response system (IWRS) and Interactive voice response system (IVRS) are to be conducted to record the subject visit as per study requirements. The investigational product is the most crucial part of a clinical trial, and the study organizer has to reserve the same in the right condition and further maintain the essential temperature logs. Clinical trial coordinator certification is also kept up to record. Coordinators should collect all primary data such as stop and start date, severity, administration route, and consumption of medicine by the subject in case of serious adverse events (SAE’s) or adverse events (AE’s). The study coordinators must look after all central and local lab reports all over the clinical trial and take PI signatures on the news to keep it as a document that the PI reviewed them.  

3. After closing the clinical trial: The study coordinators should check all the documents and clinical trial coordinator certification before closing the clinical trial and there on update all the documents. The Clinical research associate or CRA will review and verify all the materials on the day of closure of the clinical trial. The clinical research coordinator, after that, helps in archiving all the documents at the site, when the verification by CRA is complete. This site further maintains all the study associated records for about 15- 20 years. 

So it is clear that the clinical research coordinator plays a crucial role at the site level in running a clinical trial, forming clinical trial coordinator certification, and acts as a connection between EC, investigator site, and the sponsor. All clinical trials have the approval of the present Institutional Review Board. Medical care and decisions are the duty of physicians, dentists, and health care professionals. Every individual working in a clinical trial is certified by experience, training, and education. At CCRPS, we offer both CRC certification and free ICH GCP certification. Check below for our additional articles about CRCs.

Take courses from CCRPS and learn more on how to become a clinical research professional. Explore our Pharmacovigilance Certification to understand drug safety and adverse effects, or our CRA training to delve into clinical research associate roles. Those interested in supporting roles can consider the Clinical Trials Assistant Training. For advanced careers, our Advanced Clinical Research Project Manager Certification and Advanced Principal Investigator Physician Certification provide in-depth knowledge and skills. Also, our Medical Monitor Certification is ideal for those aiming to oversee clinical trials medically.

Significance of CITI Clinical Research Coordinator Course

The diseases that impact the world need solutions. To find aid for the physical and mental issues of this generation, the group of experts in the medical field work day and night. However, they can’t do this on their own. They need clinical research coordinators to help them find success. In this article, you will get to know the significance and responsibilities of clinical research coordinators, and why programs like the CITI Clinical Research Coordinator Course are critical to aspiring professionals and the field as a whole.

Who is a clinical research coordinator?

Basically, a clinical research coordinator works with a principal investigator in medical research. The principal investigator is responsible for large aspects of the project, such as securing grants and writing protocols, while the clinical research coordinator is responsible for the day-to-day operations of research. Some tasks include:

• Maintaining records and documents

• Recruiting patients

• Ensuring trials are following protocol

• Keeping the principal investigator informed on developments

• Managing supply inventory

The clinical research coordinator needs to complete a variety of tasks, but overall they need to have strong communication and organization skills. For those looking to advance in this role, the Advanced Clinical Research Project Manager Certification might be of interest.

More about the Clinical Research Coordinator Course

Being a clinical research coordinator is not easy. Thus, education and re-education is critical to field professionals.

Many different institutes and universities all around the world offer courses, but the CITI clinical research coordinator course stands out. The course is balanced and well-thought out. Students get to learn about ethics as well as the responsibilities of the clinical coordinator. The institutes do not only teach textbook knowledge, but they also encourage practical knowledge. For a comprehensive learning experience, students might consider exploring related certifications like Pharmacovigilance Certification or Clinical Trials Assistant Training to gain insights into different aspects of clinical trials. Those in more specialized roles may find the Advanced Principal Investigator Physician Certification and Medical Monitor Certification to be valuable additions to their educational pathway.

If you feel inspired, check out their course page here. If you want to compare options, try CCRPS. We offer affordable, ACCRE accredited courses dedicated to clinical research coordinators. Similarly, our courses are written by real professionals that know how to help someone stand out in the field. Still not sure yet? Below are some of our articles that will help you better understand clinical research and make an informed decision.

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

A study coordinator is the backbone of any research project. They are responsible for ensuring that all the elements of the study further the goals of the study, or the research objective. A study coordinator’s foresight and attention to detail are critical to the success of every trial.

Role Of A Study Coordinator

The role of a study coordinator is broad and includes the following:

In the planning stage: ensure that the plan is comprehensive enough to cover all aspects of the study and that various processes and elements of the study are linked. For those looking to become a study coordinator, the Clinical Research Coordinator course can provide essential training.

At the time of execution: ensure the availability of funds, apparatus, infrastructure, etc. required for the study. Further, they also have to ensure that the study flows promptly. Knowledge of ICH-GCP standards, covered in our certification course, is crucial here.

When various elements of the study are near to completion: the study coordinator will have the role to align them in a planned manner.

At all stages for research: a study coordinator ensures that research ethics are maintained, and there is no violation of any code of conduct.

Determine the Standard Operating Procedures (SOP) to be followed in a study. The Advanced Clinical Research Project Manager Certification can help develop the skills needed to define and manage SOPs effectively.

Work opportunities for a study coordinator

In many countries, such as India, study coordinators are a relatively new career route and hence acutely unexplored. However, considering the growth in research and development areas, it is pretty evident that there is an increasing demand for them. Presently, the industry needs study coordinators while only a handful of them exist.

Due to this demand-supply gap, the monetary compensation of such positions has been very high. Research by Salary.com contends that the median salary of a clinical research coordinator is around $63,330. However, based on the type of study, the range may vary from as low as $2,000 per month to as high as $4,500 per month. Those interested in expanding their career options might consider training as a Clinical Trials Assistant, or specialize further with the Advanced Principal Investigator Physician Certification or Medical Monitor Certification.

Importance

Every field of work needs consistent education, and there's always a scope for enhancement. The area of work of a study coordinator is no exception. The sky is the limit, and each training program is a step towards reaching perfection.

A study coordinator training program focuses on developing individuals to perform the roles mentioned above, in addition to other roles that may be expected from a study coordinator.

For example, regulations and code of ethics governing the respective field of study may also get updated from time to time. In such cases, it becomes necessary for the coordinators to obtain a basic understanding of the changes and implement them in a study.

Moreover, certain organizations may require applicants to have taken certain training courses before considering them for a position. Thus, it has become evermore important for hopeful professionals to take the right training courses.

Who Will Provide The Training?

Depending on the area of study, various institutions, or people with immense experience in the relevant field may provide training.

For example, an organization may organise EA training for its employees from experts in the industry. Other examples of are specialized training courses for coordinators, such as the Clinical Research Coordinator (CRC) training provided by the CITI Program.

Further, various universities run comprehensive and dedicated courses for imparting study coordinator training. Some such institutes are Clinical and Translational Science Institute (CTSI), which provides basic coordinator training, and ACRP, which provides Certified Clinical Research Coordinator (CCRC) training.

Conclusion

The field of a study coordinator is a career that has immense potential yet to be explored. More trained professionals can prove to be very valuable assets to the research processes. At CCRPS, we offer ACCRE accredited training specialized for study coordinators. In addition, we have complied articles below to help you better understand the complex aspects of clinical research.

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

If you think practically, then you will find that nothing in this world comes for free. But if you have a passion for clinical research and need to learn on a budget, here are some ways you can enhance your understanding without breaking the bank.

To understand how you can learn for free, it’s first important to understand the typical trajectory of a clinical research coordinator:

• A person seeking clinical research coordinator training should complete high school. There they learn must-have all the science subjects like physics, chemistry, and biology.

• After high school, institutes for professional clinical research coordinator professionalism offer programs that are essential for later.

• In addition, one can get an experience graduate certificate from an online source. This would help the person reach their career goals faster.

• Alternatively, they can complete a bachelor's degree of science.

• After completing the bachelor's degree, a master's degree is needed for some of the higher pay-grade positions.

How to get free clinical research coordinator training?

If looking at the education requirements for a clinical research coordinator makes you dizzy, you’re not alone. Becoming a clinical research coordinator takes a lot of time and money. That is why many students turn to scholarships and healthcare programs to help pay their tuition.

On the other hand, there are many websites that offer free or affordable information and training for aspiring professionals. While they can’t replace a formal education, they can supplement your resume and knowledge. While some important topics include clinical data management, pharmacovigilance, and regulatory authorities, you should strive for a comprehensive understanding of the field. At CCRPS, we offer affordable courses designed for clinical research coordinators as well as free ICH GCP training. These can help you build your resume and land the position you want.

In addition, it is really important to keep updated with new clinical research headlines. Below, I have complied some articles that aspiring professionals might find useful. The best thing you can do for your education is to start now and not later.

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

A clinical research coordinator or CRC is a highly trained professional, whose expertise is crucial to all medical research work. Although a CRC works under the constant guidance of a principal investigator, they are responsible for the day to day trials and clinical operations. Thus, this profession can be quite challenging but rewarding.

However, getting into the crew of CRCs is not an easy task. A particular individual may need to prepare for a while to be selected for such a post. In this segment, you can learn all the aspects to becoming a successful CRC.

What does a Clinical Research Coordinator do?

A clinical research coordinator or CRC is a highly trained professional, whose expertise is crucial to all medical research work. Although a CRC works under the constant guidance of a principal investigator, they are responsible for the day-to-day trials and clinical operations. Thus, this profession can be quite challenging but rewarding.

However, getting into the crew of CRCs is not an easy task. A particular individual may need to prepare for a while to be selected for such a post. In this segment, you can learn all the aspects to becoming a successful CRC through specialized training such as the Clinical Research Coordinator course.

What does a Clinical Research Coordinator do?

The field of medicine is always advancing. In the world of medicine, new knowledge is indispensable. So, the professionals of the medical branch are always looking to conducting experiments that can lead them to new cures and successes. Among clinical research professionals, clinical research coordinators are at the front lines of research operations and analytics.

The duties of a CRC are to plan and initiate a study or experiment the board has approved. During the phases of the project, they must maintain communication between their site and institutional organizations. The CRCs are eligible to do the research and reviews. Additionally, they can choose to hire potent candidates for their purpose. Understanding and adherence to ICH-GCP guidelines are crucial for ensuring compliance and ethical conduct in their studies.

How can you be a successful clinical research coordinator?

The job of a clinical research coordinator is not an easy one. However, with enough hard work and patience, one can become eligible for the post. Although, individuals who aspire to become a clinical research coordinator are advised to understand the basics and keep educating themselves if they want to become a trusted professional. Continual education and certification, such as the Pharmacovigilance Certification and Clinical Trials Assistant Training, can provide essential knowledge and skills required in this evolving field.

Additionally, for those looking to further their careers, the Advanced Clinical Research Project Manager Certification and Advanced Principal Investigator Physician Certification are excellent resources to consider. Those interested in overseeing clinical trials and research safety might consider the Medical Monitor Certification.

Here are the requirements to become a successful clinical research coordinator:

1. To apply for this post and profession, the candidates need to have a background that is related to the field of medicine or biology. The general preference for applying is to have a bachelor's degree in microbiology or medical technology.

2. Some positions require individuals who have a master’s degree on top of their bachelor’s degree. So, you might need to invest more time into your education if you want to work with certain firms or reach a higher pay-grade.

3. Preparing yourself for the job is crucial. As this job is a challenging one, individuals might need to develop and train themselves for quite some time to do well. For young training candidates, clinical trial coordinator training is shown to be quite a useful resource. At CCRPS, we offer affordable training courses developed by real professionals and accredited by ACCRE. If you are looking to learn more about clinical research and specific positions, CCRPS can be the perfect starting point.

A step towards the development of humankind

Medical science has experienced great expeditions over the past few decades, and all of that has help benefit society in some way or the other. Thus, becoming a part of a research team is a commendable task indeed.

Becoming a clinical research coordinator isn’t easy. A CRC must have an eye for detail and need to continually polish their skills. Moreover, experience and education is a determining quality that can set a good CRC apart from the rest in the lot. If you’d like to start your education, check out CCRPS. Our courses and articles will help you find the tools to succeed in clinical research.

Take courses from CCRPS and learn more on how to become a clinical research professional.

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