DGM - Clinical Trials - Pharma (10-16 yrs)
- Experience in Clinical Trials /Clinical Research
- Provided scientific inputs on the feasibility of new proposals of clinical trials from clients across the globe.
- Coordinated directly with the study sponsor for all project related matters
- Managed to provide inputs/review of the protocols, CRFs, ICFs, study reports, QA queries and clinical updates for clinical studies.
- Ensure the successful conduct of regulatory inspections and client audit(s).
- To constitute the DSMB (Data Safety Monitoring Board), assist the DSMB meetings and discuss the study data with DSMB members. Active participation to discuss the several safety aspects of trials with DSMB members.
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