Job description

As a Clinical Study Manager, you will be responsible for the planning, coordination, execution, and oversight of clinical studies for Class I and Class II medical devices, ensuring compliance with applicable regulations and quality standards.

Your responsibilities include:

• Lead the operational management of clinical studies from study start-up through close-out.


• Develop, review, and maintain clinical study documentation, including clinical protocols, informed consent forms, study plans, monitoring plans, and clinical reports.