Contractspecialist Klinisch Onderzoek
Core
Full-time Contract Specialist for Clinical Research managing the entire contractual lifecycle of clinical studies from preparation to finalization.
Role type
Contract Specialist (Clinical Research)
Builds
Clinical Site Agreements (CSA's) and location-specific legal agreements for clinical studies
Domain
Clinical Research / Pharmaceutical / Biotechnology
Deliverable
client delivery
Required skills
Contract negotiation, Legal agreement drafting, Stakeholder relationship management, Risk identification, Regulatory compliance knowledge, Project management
Preferred skills
Experience in clinical research, Contract management, Pharmaceutical sector, French language
Technologies
Clinical Site Agreements (CSA's)
Responsibilities
Draft, review, negotiate, and finalize Clinical Site Agreements (CSA's) and other location-specific legal agreements; Act as the primary point of contact and subject matter expert for Belgium regarding CSA strategy and timing; Negotiate within approved contract and budget templates; Build strong relationships with research sites and external stakeholders; Identify and assess legal, financial, and operational risks; Collaborate with internal departments to align study start activities with contractual processes; Stay updated on local laws and regulations impacting clinical research contracts.
Seniority
Entry to Mid-level (Starters and experienced candidates encouraged)