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HainautHybridHours negotiable<3months
This role is within a leading global Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies. You will be part of a team dedicated to one sponsor, a global pharmaceutical or biotechnology company that is an industry leader within its therapeutic area. This is a part-time opportunity.
What you do
- Perform on-site and remote monitoring visits
- Ensure protocol compliance, patient safety, and data integrity
- Review CRFs and source data for accuracy
- Verify informed consent procedures are followed
- Manage investigational product accountability
- Write and submit monitoring visit reports
- Track issues and ensure timely follow-up with sites
- Maintain eTMF/ISF documentation compliance
- Support audits and inspections
- Update CTMS and study systems with accurate data
What they ask
- Bachelor’s degree in Life Sciences, Nursing
- 3+ year clinical research experience or relevant academic experience
- Knowledge of GCP, ICH, and clinical trial processes
- Strong communication and organizational skills
- Ability to work independently and in teams
- Fluent in English
- Experience in CNS/Neuro studies is a big advantage
How to apply
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