Related skills
clinical trials site management budget ich-gcp irb/ec📋 Description
- Supports execution of company-sponsored clinical trials, ensuring timelines.
- Oversees feasibility, setup, conduct, and closure per ICH-GCP and SOPs.
- Primary site contact for trial sites; manages site relationships.
- Contributes to development of essential trial documents and PMCF planning.
- Interfaces with IRBs/ECs, vendors, and cross-functional teams.
🎯 Requirements
- Bachelor's degree in Life Science, Physical Science, Nursing, or Biological Science.
- BS with 4+ years, MS with 3 years, PhD with 2 years preferred.
- Previous clinical research or equivalent experience required.
- Industry certifications (CCRA/CCRP/RAC, etc.) preferred.
- Strong understanding of ICH-GCP, regulatory requirements and SOPs.
- Excellent written and verbal English communication; leadership skills.
🎁 Benefits
- Hybrid work model in Diegem, Belgium.
- Global CRO environment focused on quality and professional development.
- Client-facing role with growth opportunities and supportive culture.
- Equal opportunity employer.
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