1. Responsible for the management of designated clinical trials including investigator selection, analysis of potential patient recruitment, preparation of trial related documentation (protocols, Case report forms, investigators brochures, consent documents, letters of agreement, confidentiality agreements), organizing Ethics committee submissions with follow through to ensure successful outcome.
Salary:
Best In The Industry
Industry:
Pharma / Biotech / Clinical Research
Functional Area:
Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category:
R&D
Role:
Chemical Research Associate/Scientist
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