Location
Belgium, Belgium, Belgium
Posted
July 02, 2026
Job Description
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...