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Freelance SCRA - Turkey - 0.5FTE
ProPharma
Leiden · HybridSenior (5–10 years)Part-time, ContractPosted today
About the job
What you'll do
The Senior Clinical Research Associate is responsible for clinical monitoring activities, including site initiation, interim, and close-out visits to ensure protocol and regulatory compliance. They also manage site personnel, oversee data integrity, and maintain essential study documentation.
What they're looking for
Candidates must have a Bachelor's degree and over 5 years of experience as a Clinical Research Associate. Proficiency in clinical trial regulations, GCP, and electronic systems like EDC and CTMS is required.
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