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Clinical trial design concepts and parametersĪ sound grasp of the clinical trials process is similarly a must for senior professionals in the team. The CRPM has final responsibility for ensuring that all documentation necessary for clinical research regulatory compliance is maintained and updated as needed. As clinical trials progress, any changes to the study trial protocol, consent procedures or data management system must likewise first be reviewed and approved by the IRB. Part of Title 21 regulatory compliance requires nearly all clinical research studies to first be approved by an Institutional Review Board or IRB (also called an Ethics Committee). Clinical research across the US must conform to the requirements of Title 21.

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The ICH-GCP principles are mirrored by Title 21 within the US FDA’s Code of Federal Regulations (CFR).

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One of the first things every clinical research professional learns is the importance of adhering to the principles and policies of good clinical practice, as outlined in the ICH-GCP-these guidelines set the framework for carrying out research in a manner that prioritizes the safety and welfare of human subjects and the quality and integrity of clinical data. ICH-GCP guidelines, Title 21 of FDA CFR and IRB compliance In broad strokes, a CRPM candidate likely already has a knowledge base and skill sets in the following areas: 1. In addition, a professional at this stage has usually acquired a good working knowledge of the planning and oversight required for a clinical research study. The CRPM journey, Part 1: Research and administrative skillsīy the time a clinical research professional is eligible to apply for a CRPM position, s/he has typically developed a range of competencies in the day-to-day running of clinical trials. The final sections address how the Advanced Clinical Research Project Manager Certification or ACRPMC facilitates the transition to a CRPM role. For conceptual convenience, the process is discussed in two parts – Part 1 centers on the research and administrative skills needed for a CRPM, while Part 2 revolves around expertise in project management. Irrespective of where you are along this path, the remainder of this article charts a clinical research professional’s journey of growth in developing into a competent CRPM. A typical CRPM has a bachelor’s (or master’s) degree in life science, combined with four to five years’ experience in one or more clinical research roles such as CRC, senior CRA or QPPV (Qualified Professional in Pharmacovigilance). So, what does it take to qualify and be recruited as a Clinical Research Project Manager? The road-map to becoming a CRPMĮven if you’re new to the field of clinical research, you’ve probably guessed by now that becoming a Clinical Research Project Manager takes both qualifications and experience. In the process, a CRPM also mentors junior team members, including CRAs and CTAs.Įvidently, a career as a CRPM is rewarding, but also demanding. The CRPM plays a leading role in planning, implementation and ongoing monitoring of live clinical trials. Thus, the CRPM must balance the expectations of the funding organization in a clinical research study (pharmaceutical company, governmental agency, university research division or other entity) with the needs of the team, including Principal Investigators (PIs) and co-PIs, Clinical Research Coordinators (CRCs), Clinical Research Associates (CRAs), Clinical Trial Assistants (CTAs) and other site staff.

An overview of the CRPM profileĪ Clinical Research Project Manager is the liaison between the study sponsor and the clinical research team.

The role of a CRPM is to provide leadership during the clinical trial of new drugs, with the overarching goal of ensuring that the clinical trials process is completed within the stipulated time-frame and allocated budget, while maintaining the highest standards of research quality and scientific integrity. According to ‘’, remuneration for this profile ranges from $84,168 for early-career to $120,501 for experienced Clinical Research Project Managers, with a mid-career median of $107,649.Ī Clinical Research Project Manager (henceforth CRPM) is also known as a Clinical Research Manager or a Clinical Trial Manager.

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Clinical Research Project Manager - A Full Guide To Becoming a Clinical Trial Project ManagerĪs of mid-April 2022, top recruitment platform ‘’ lists 6,026 openings for Clinical Research Project Managers across the United States.