Senior Site Activation Specialist - Belgium
IQVIA · Charleroi, Belgium +6 more
Clinical OperationsFull-timeCompany career page
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Role summary
IQVIA seeks a freelance senior site activation specialist based in Belgium to support clinical trial start-up and site management activities. The role involves EU-CTR compilation, regulatory submissions, document management, and site activation oversight across multiple investigative sites for approximately six months.
What they're looking for
- Based in Belgium with strong local regulatory environment knowledge
- 2–3+ years of site activation, study start-up, or clinical research experience
- Bachelor's degree in Life Sciences or related field
- Solid knowledge of clinical trial start-up processes and regulatory requirements
- Experience managing site documentation and submission processes
- Fluent in Dutch or French and English (written and spoken)
- Strong attention to detail and ability to manage multiple sites and timelines
What you'll be doing
- Serve as primary point of contact for assigned investigative sites
- Execute feasibility assessments, site identification, and activation activities per SOPs and regulations
- Prepare, review, and manage essential site and regulatory documents for completeness and accuracy
- Maintain tracking tools, timelines, and internal systems with accurate project data
- Monitor site activation progress and performance metrics, reporting findings to stakeholders
Privacy & handoff
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.