Acts as the bridge between the pharmaceutical sponsor and the clinical trial sites (hospitals). They ensure trials are conducted ethically and safely
Monitor clinical trial sites to ensure compliance with the Study Protocol. Verify data accuracy against source documents (Patient records). Ensure adherence to Good Clinical Practice (GCP) and ICH guidelines.
Knowledge of Clinical Trial Management Systems (CTMS). Strong understanding of FDA/EMA or CDSCO (India) regulations. Education: Bachelor’s/Master’s in Life Sciences, B.Pharm, or Nursing
Mandatory Skills
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