Clinical Project Manager

Clinical Project Manager (CPM)

Location: France or Belgium (Fully remote)

Availability: Immediate

Work Model: 1 FTE

Contract Period: 6 Months

Company Overview

Apsida Life Science has partnered with a premier medical device and MedTech specialist Clinical Research Organization (CRO) in Europe. They are currently seeking an experienced Clinical Project Manager to join their team.

The Opportunity

• Lead and manage clinical studies within the MedTech and medical device space.
• Ensure all projects meet rigorous MDR and ISO standards.
• Collaborate with a specialist CRO team to deliver high-quality clinical trial results.
• Strong background in GMP (Good Manufacturing Practice) to ensure quality standards in device clinical investigation and manufacturing.

What you need:

• A Bachelor's or Master's degree in Life Sciences, Biomedical Engineering, or a related technical field.
• Proven experience as a CPM within a CRO environment, specifically focused on medical devices.
• Deep functional knowledge of Medical Device Regulation (MDR), ISO standards, and medical device clinical trials.
• Fluency in French.
• Immediate availability.

What You Will Get:

• Total ownership over your clinical sites and regulatory milestones.
• A competitive, all-inclusive industry standard rate.
• The chance to work with a highly innovative medical device specialist.
• A flexible remote or hybrid work model across Europe.

If you are interested in learning more, please reach out to Linda Goba at Apsida Life Science

Email: [email protected] Website: www.apsida.co.uk Phone: 44 (0) 744 134 2145

Apsida Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA) & Pretoria (South Africa) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost effective, high quality and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.

Website: www.apsida.co.uk