Clinical Project Manager - Class III Medical Device

Our Client is seeking a dedicated and proactive Clinical Project Manager specialising in Class III Medical Devices to join their team in Munich, Germany. As a Clinical Project Manager, you will play a crucial role in overseeing clinical project management and day-to-day operations throughout the study life-cycle, ensuring compliance with protocols and regulations.

Key Responsibilities:

Manage and coordinate clinical operations from start-up to close-out phases.
Contribute to the development and writing of clinical study documentation.
Liaise with regulatory authorities for study-specific document submissions.
Maintain accurate study documentation and Trial Master File (TMF).
Act as the primary contact for study sites, ensuring protocol compliance.
Conduct monitoring visits and resolve data discrepancies.
Collaborate with cross-functional teams for successful study execution.

Qualifications and Experience:

Bachelor's degree in Life Sciences, Nursing, or related field.
Minimum of 2 years of experience as a Clinical Project Manager in the medical device industry.
Proficiency in ISO-14155, ICH-GCP, MDR, and associated guidelines.
Experience with electronic data capture systems.
Strong attention to detail and organisational skills.
Excellent communication abilities.
Proficiency in English required; German language skills are a plus.

What's On Offer:

Dynamic and innovative work environment.
Professional growth opportunities.
Collaboration with a skilled and passionate multinational team.
Up to €80,000 per annum and benefits package.

If you are a motivated Clinical Project Manager with a background in Class III Medical Devices, we invite you to submit your CV and cover letter to be considered for this exciting opportunity. Join Our Client in their mission to bring innovative treatment solutions to patients.