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Clinical ResearchPharmaceuticalsMid
Clinical Research Associate II
Amsterdam, NetherlandsPermanent€55,000 – €70,000Posted 1 week ago
About the role
Monitor Phase II–III oncology trials across European sites, ensuring data quality and GCP compliance.
What you’ll do
- Conduct site initiation, monitoring, and close-out visits.
- Verify source data and resolve queries with site staff.
- Ensure trials run to protocol, GCP, and local regulations.
- Maintain the trial master file to inspection standard.
What you’ll bring
- 3+ years of on-site monitoring experience.
- Working knowledge of ICH-GCP and EU CTR.
- Willingness to travel up to 60% across the EU.
- Life sciences degree; fluent English, second EU language a plus.
Bektin is an equal-opportunity partner. We present every qualified candidate on merit and keep your details confidential until you approve a submission.
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