A leading global mid-size CRO in Helsinki is seeking a Study Coordinator (Freelance/Contractor) to support clinical studies. The role includes data entry, assisting with patient recruitment, and managing study tasks under the supervision of the Principal Investigator. Candidates should have a clinical or life science background, GCP certification, and familiarity with eCRF/EDC systems. Finnish language skills are mandatory. Join a dynamic team dedicated to advancing clinical research and improving patient outcomes.
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