1. Overseeing all implementation all project specific clinical data as a QC.
2. Coordinate with protocol preparation.
3. Preparation of clinical study reports (CSR), Project summary.
4. ICF Reviewing and obtaining of ICF.
5. Reviewing of Trial Master File.
6. Coordinate with the Volunteer Information Management System (VIMS).
7. Dosing and supervision of Investigational Product.
8. Preparation of clinical reports.
9. Preparation and compilation Case Report Forms (CRF) of pilot and pivotal
10. Thorough with the in-house SOPS, ICR and GCP guidelines.
Desired Candidate Profile
Education-
UG: B.Pharma - PharmacyPG:M.Pharma - Pharmacy
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