- Recording the relevant details in the appropriate workbooks.
Preparing detailed reports immediately at the end of the task relating to the project or as required by your supervisors.
Recruit patients & obtain their consent for trials.
Update Case Record Forms (CRFs) daily & manage external audits
Strict adherence to GLP, ICH & other Regulatory requirement.
B.Pharm/M.Pharm/M.Sc (Life sciences) with 1-2 Yrs experience as CRA in a reputed CRO dealing with Clinical Trials.
Training in GCP.
Relevant exp. in conducting multi-centric clinical trials.
Knowledge of processing & reporting AE/SAE events during CTs.
Coordinate CT supplies & collection/shipment of biological samples
Keyskills
Desired Candidate Profile
Education-
- Please refer to the Job description above