(CRCPro™) Clinical Research Coordinator (CRC) Professional Certification Program
Today, clinical trials have to be conducted in line with federal, local, and international standards. To ensure your organization or team members know what steps to take to ensure Good Clinical Practice is followed, getting certified as a CRC can be beneficial under such circumstances. At Biopharma Institute, we offer Clinical Research Coordinator online courses for professionals who work in clinical research, healthcare, and pharmaceutical industries.
What is (CRCPro™) Clinical Research Coordinator (CRC) Professional Certification Program?
(CRCPro™) Clinical Research Coordinator (CRC) Professional Certification Program is offered by Biopharma Institute.
The CRCPro™ – Clinical Trials Coordinator – Professional Certification Program is a credential that is awarded to a clinical research coordinator who has demonstrated training proficiency as well as met the eligibility requirements.
Who Should Get CRCPro™ Certified?
If you have been tasked to coordinate, supervise, and/or support the facilitation of a clinical trial on behalf of an investigator, it is recommended that you get CRCPro™ certified. An investigator site sees recruits and treats patients enrolled into a clinical trial. In addition, it is beneficial for individuals, who are involved in the research of pharmaceuticals, biologics, and other devices, to participate in these programs.
CRCs that have a few years of experience should get certified as it is a good way to stand out from the crowd when it comes to advancing one’s career. Getting certified is also ideal for professionals who plan to discuss a raise with their employers. It’s hard for superiors to argue when their employees are well qualified. What’s more, sponsors prefer to work with investigators who have certified or experienced CRCs on staff.
Overview of CRCPro™ Coursework Details
Wondering how a typical CRCPro™ coursework looks like? Generally speaking, you can expect your courses to cover:
- ICH-GCP Good Clinical Practice
- Clinical Trials: Preparing for an Audit or Inspection
- ICH E6(R2) GCP Training for Investigator Site Personnel
- Overview of ICH E8(R1): General Considerations for Clinical Studies Guideline
- Good Documentation Practices and ALCOA-C
- HIPAA Training for Clinical Trial Professionals
How to Know if You are Eligible to Become a CRC
For starters, you need to acquire a bachelor’s degree (or higher), as most positions include this as a minimum requirement for hiring. While it is possible for applicants (CRCs) to enroll in these programs without needing to meet additional requirements, having clinical research experience is an asset. A background in medicine, pharmacy, nursing, and the life sciences will add to your advantage.
The next set of requirements includes strong speaking and writing skills. CRCs need to communicate effectively with doctors, researchers, and other program participants. Below is a quick checklist you can use to determine your eligibility:
- You have a letter of recommendation from a client or employer
- You have a record of experience in completing relevant CRC tasks
- You have documents of past trainings
- You have between one to three years of experience working in clinical research
Prepare for the CRC Certification at Biopharma Institute, Today!
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If you’d like to find out more about our CRC training, you can contact our customer service team by sending an email to firstname.lastname@example.org or calling (888) 424-6576.