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Clinical Research Manager (Local Trial Manager) - France - FSP

Parexel•France•🌍 Remote
Full-timeSenior
👁️ 0 views•📝 0 applications•Posted 9/27/2026•Expires 11/26/2026
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Job Description

When our values align, there's no limit to what we can achieve. At Parexel , we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel , contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

About Parexel Parexel is a leading global clinical development partner delivering insights driven clinical and consulting solutions to the life sciences industry.

With 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient focused clinical trials that broaden access and make research a care option for anyone, anywhere.

We work with focus, agility, and shared purpose, moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research.

We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart®.

About the Role

We are seeking a Clinical Research Manager (CRM) to join our team in a home-based capacity in France. As a Clinical Research Manager, you will play a pivotal role in the successful delivery of complex oncology clinical trials for a top pharmaceutical client.

This position is responsible for the end-to-end management and performance of assigned protocols, ensuring compliance with ICH-GCP, local regulations, client requirements, and quality standards.

Working across study start-up, maintenance, and close-out, you will provide strategic oversight of trial execution, site performance, vendor management, and CRA activities. You will collaborate with cross functio

Required Skills

oncologyICH-GCPlocal regulationsclient requirementsquality standardstrial executionsite performancevendor managementCRA activities
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