Clinical Research Associate I/ Clinical Research Associate II
Related skills
sops ich-gcp investigators📋 Description
- Monitor clinical studies at investigative sites per protocol and ICH-GCP.
- Ensure data are recorded and reported per SOPs and regulations.
- Coordinate site setup, regulatory submissions, and initiation visits.
- Identify investigators and support study start-up activities.
- Travel domestically up to 50-60%; some roles may require international travel.
- Collaborate with study teams to mitigate risks and ensure quality.
🎯 Requirements
- Life science degree or equivalent experience.
- 2+ years as a CRA in CRO/pharma/biotech; site management experience.
- Domestic travel up to 50-60% (international travel may be required for some roles).
- Fluency in English and Dutch; French a plus.
- Excellent communication and organizational skills; client-focused.
- Oncology monitoring experience a plus; study start-up experience preferred.
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