IQVIA · Amsterdam, Netherlands +3 more
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
This role coordinates site activation activities across clinical research studies in the Netherlands, serving as the primary contact between investigative sites, project teams, and internal departments. The position requires Dutch language proficiency, experience with local submissions and contract negotiations, and responsibility for regulatory document preparation, compliance monitoring, and timeline management in a home-based arrangement.
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.
This role is listed from an approved source. RoleLantern checks that the application link is live and how recently the role appeared — the employer has not confirmed it directly on RoleLantern.
Upload your CV to see which of this role's requirements your background supports, where there may be gaps, and what needs clarification. Private by default — we never sell your CV.
See my match