Clinical Project Manager (IVD experience required)

Share Publication date 1 July 2026 Department Quality, Regulatory and Clinical Affairs Country Belgium Location Mechelen Work arrangement Hybrid Travel percentage 10% (max) Function type Full-time Contract type Contractor Experience required

2-5 years of relevant experience working in Clinical Operations in the pharmaceutical/biotech industry/ medical device and/or a CRO.

Experience with trial master file organization, regulatory documents, inspection preparation/readiness (site and Sponsor) and all aspects of trial and vendor management perferred.

High degree of competence in all aspects of a clinical research program is required.

Strong practical knowledge of compliance and regulatory environments (US, EU and rest of world) is required.

Experience in IVD (clinical ) development and validation studies is required.

Experience in Companion Diagnostics projects is an asset.

Proven experience with KOL-, CRO- and i...