Clinical Research Associate I/ Clinical Research Associate II
Related skills
clinical trials site monitoring regulatory submissions oncology biopharma📋 Description
- Monitor progress of clinical studies at investigative sites.
- Ensure studies follow protocol and ICH-GCP.
- Coordinate site setup and monitoring, including investigator identification.
- Manage regulatory submissions and initiation/pre-study visits.
- Remote-based role with travel to sites for visits.
🎯 Requirements
- Life science degree or equivalent experience.
- 2+ years as CRA in CRO or pharma/biotech; site management experience.
- Availability for domestic travel; international travel may be required.
- Fluent in English and Dutch; French a plus.
- Oncology monitoring experience a plus.
🎁 Benefits
- Remote-based role with travel to sites.
- Travel up to ~50-60% depending on role.
- Good work-life balance.
- Smaller CRO with direct line management support.
- Opportunity to influence protocol outcomes in oncology/rare diseases.
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