Clinical Project Manager Medical Devices

Netherlands/Europe

About Qserve

Qserve is a global consulting company, focusing on the medical industry. We help medical device & in-vitro diagnostics manufacturers worldwide with market access, medical device registrations & approvals, in-country representation, achieving & maintaining regulatory compliance and clinical trails. Our headquarters are located in the Netherlands (Arnhem) and we have local presence in Germany, Belgium, United Kingdom, USA and China. With approximately 100 colleagues, we work together in global teams. Our organization is rapidly growing and has ambitious plans for the future.

Responsibilities

The Clinical Project Manager (CPM) is responsible for the planning, setup and execution of clinical investigations for medical devices and in-vitro diagnostic devices at Qserve’s Contract Research Organization (CRO). In close cooperation with the sponsors (medical device manufacturers), the CPM ensures the development of the necessary study documents, secures ethics approval and competent authority approval, and manages the study from the start to the end. The CPM works closely together with other CPM’s and leads small diverse teams of in-house and contract Clinical Research Asso

“Global reach, practical approach, experienced team”

Interested?

Getting excited about a career as a consultant in the dynamic and innovating world of medical devices? Then please submit your resume and letter of motivation to careers@qservegroup.com or use our application form on our website: https://qservegroup.com/en/careers.

For more information about our company, you can always visit our website (www.qservegroup.com) or contact our HR department at +31 20 78 82 630.

The position is mainly office-based at our Headquarters in Arnhem (The Netherlands); we expect our consultants to work at the client location as well as that we offer flexibility to work from homethis position requires international travel up to 20% of the time.