The clinical research coordinator is one who has gone through and has gotten a clinical research coordinator certification to fully function and practice as one.
Clinical research coordinator (CRC) is sometimes called a clinical trial manager because they play an integral role in all kinds of medical studies. Working under the direction of the principal investigator who designs, conducts, and manages clinical trial, the clinical research coordinator supports, organizes, and facilitates the daily activities of the clinical trial.
A Clinical research coordinator manages, oversees, executes tasks and day to day clinical trial activities, as well as works in conjunction with sponsors, departments, and institutions to manage finances, obtain compliance, and work through personal issues. The responsibilities include the planning and management of the following initiatives; study, enrollment, maintenance, and training. It also deals with compliance with the institutional, state, and federal regulations.
They engage directly with the trial participants, screening them for eligibility. They help develop and implement recruitment strategies and work with all the available teams during the trial period. They carry our experiments, medical studies, and clinical researches. A CRC has a lot of links within labs, medical centers, and research hospitals, due to the evaluation of research protocols and the seeking of approval from regulatory committees.
To get certified as a CRC you must have gotten at least a four-year bachelor's degree in medical technology, public health administration, or microbiology, with an additional two years master's degree in management positions (optional). Human anatomy, biostatistics, epidemiology, health care management, biochemistry, and mathematics, are the courses typically required. Management and communications experience coupled with interpersonal and multitasking skills are essential job skills to possess, internships and/or low entry-level jobs as health care workers or lab technicians should also be considered to get familiarised with the working environment.
To be certified as a clinical research coordinator you have to go through steps and stages.
The preparation doesn't just start from now, it starts all the way back in high school. The foundation is formed from choosing clinical research coordination combination courses in biology, physics, maths, and communications. It is then followed up with a 4 years bachelor of science degree in health sciences in clinical research administration. This could lead to an entry-level position in a clinical institution or organization. Next, gain work experience as a clinical research professional for at least a year, this is a necessary requirement to qualify for national certification.
The next step would be to obtain an online graduate certificate. To be eligible for the CRC certification exam you need to have one of the following:
A Bachelor's degree or a Higher degree in health sciences in clinical research administration and submission of a fully detailed resume that documents at least 3,000 hours of performed designated duties.
A Registered Nurse (RN), LVN, Licensed Practical Nurse (LPN), or an associate degree and a submission of a detailed report that documents at least 4,500 hours of performed designated duties.
Laboratory technician, medical assistant, or a high school diploma and submission of a detailed report that documents at least 6,000 hours of performed designated duties.
It is important to note that there may be a substitution for hours of qualifying work experience.
Certification lets you practice legally and can see you earning from as little as $48,000 to as much as $60,000 annually.
To learn more, you can take a course in clinical research coordination which will help develop and refine your skills more before you go on to get the clinical research coordinator certification.