Clinical Study Project Manager

Clinical Study Project Manager – Drive Innovation in Medical Research

Are you passionate about advancing medical research and bringing innovative healthcare solutions to the world? Do you thrive in a dynamic, fast-paced environment where collaboration and strategic execution are key? If so, we have the perfect opportunity for you!

We are looking for a Clinical Study Project Manager to lead the preparation and execution of a clinical performance study and contribute to the global registration and certification of in vitro medical devices . This role offers a unique chance to work at the intersection of R&D and clinical operations , ensuring that cutting-edge medical research is conducted to the highest standards.

Your Role & Responsibilities :

As a Clinical Study Project Manager, you will be responsible for end-to-end management of clinical studies, overseeing the process from initial planning to completion. Your key duties will include :

• Selecting, negotiating, and contracting clinical study vendors .
• Leading tenders preparation and execution with external consulting partners.
• Developing study-related documents in collaboration with internal teams and contracted CROs .
• Participating in feasibility and site selection processes for clinical studies.
• Creating and overseeing the recruitment strategy , ensuring studies meet required participant numbers.
• Acting as the main point of contact , leading and managing studies from start-up to close-out .
• Coordinating with internal and external stakeholders to ensure timely execution and budget control .
• Supporting quality assurance process implementation for clinical and medical research activities.

What We’re Looking For :

We’re seeking a proactive and detail-oriented professional with a strong scientific background and proven clinical project management experience . To succeed in this role, you should have :

Preferred (Bonus) Experience :

Candidates with additional expertise in the following areas will be given priority :

Project management of IVD studies (2+ years).

Oversight of external vendors (CROs, central labs, etc.).

Vendor and clinical site contracting for multi-center studies.

Conducting tenders (bidder selection, negotiations, contract development).

Hands-on experience in multi-center, multi-country clinical studies (CRA, Data Manager, Feasibility Specialist, etc.).

Why Join Us?

In this role, you will be at the forefront of groundbreaking medical advancements , working in an environment that values innovation, collaboration, and excellence . You’ll have the opportunity to shape the future of clinical research , lead impactful projects, and work alongside a highly skilled and passionate team.

Flexible working environment

Engaging and impactful projects

Career growth opportunities

Work with leading experts in the field

If you're ready to take on a leadership role in clinical study management and contribute to life-changing medical advancements, apply now!