CareerPlan

Contract Specialist (Experienced)

Leuven, BelgiumContract2026-10-11 → 2026-11-10
On-site

Core

Managing the full lifecycle of clinical site contracts, including drafting, negotiating, and finalizing agreements to enable study start-up.

Role type

Contract Specialist (Clinical Trials)

Builds

Clinical Site Agreements and site-specific legal agreements for clinical studies

Domain

Clinical Research / Biopharma

Required skills

Contract negotiation, Legal risk assessment, Stakeholder relationship management, Regulatory compliance knowledge, Project coordination, Attention to detail

Preferred skills

Prior contract negotiation experience, French language proficiency

Technologies

Contract lifecycle management systems, Legal templates

Responsibilities

Drafting, reviewing, negotiating, and finalizing Clinical Site Agreements; Act as first-line subject matter expert for country-specific CSA strategy; Identify and assess legal, financial, and operational risks; Coordinate with internal functional departments to align site startup activities with contractual timelines; Keep up to date with applicable local regulations impacting clinical trial contracts.

Seniority

Mid-level, hands-on IC