
Job Overview
Location
3 Locations
Job Type
Full-time
Category
Product Marketing Manager
Date Posted
April 16, 2026
Full Job Description
đź“‹ Description
- • The Clinical Compliance Manager provides GCP compliance support to clinical study teams, ensuring adherence to regulatory requirements, ICH GCP guidelines, and sponsor SOPs for the conduct of clinical studies.
- • Day-to-day responsibilities include acting as a Clinical Compliance member of clinical study teams, developing relationships with R&D personnel, conducting risk assessments, identifying and escalating compliance issues, participating in CRO/vendor governance teams, supporting audit responses and CAPA development, and leading inspection readiness activities.
- • Parexel is a global leader in clinical development solutions, supporting trials for top-selling drugs and niche therapies alike, with a mission to improve global health through empathy-driven, patient-focused work.
- • In this role, you will deepen your expertise in global regulatory frameworks, lead compliance initiatives across therapeutic areas, influence quality culture, and gain experience in risk-based compliance strategies and inspection readiness for international clinical trials.
About Parexel International Corporation
Parexel provides global biopharmaceutical services, managing Phase I-IV clinical trials, regulatory consulting, market access, and real-world evidence studies for drug and device development. The company supports sponsors in trial design, site selection, patient recruitment, data management, biostatistics, pharmacovigilance, and health economics. Operating in over 100 countries, Parexel integrates therapeutic expertise with technology platforms to accelerate approvals and improve evidence generation. Services span oncology, neurology, rare diseases, and vaccines, combining decentralized trial capabilities, digital health tools, and post-marketing surveillance to optimize development timelines and commercial success.
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