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GVP Compliance Specialist - Clinical Consulting

ProPharma Group
Western, IL Full Time
POSTED ON 3/3/2025
AVAILABLE BEFORE 3/30/2025

About the Role

As a seasoned professional in clinical consulting, we are seeking a highly skilled GVP Compliance Specialist to join our team at ProPharma Group. In this pivotal role, you will be responsible for ensuring compliance with Good Pharmacovigilance Practices (GVP) and Good Clinical Practice (GCP) regulations.

Job Responsibilities

Requirements

Benefits

About Us

At ProPharma Group, we are committed to empowering biotech, med device, and pharmaceutical organizations to advance scientific breakthroughs and introduce new therapies. As the world's largest Research Consulting Organization (RCO), we partner with clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, we offer a comprehensive suite of fully customizable consulting solutions that de-risk and accelerate our partners' most high-profile drug and device programs.

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