Job designation-Clinical Research Associate
Job descrption-Monitor the compliance with the clinical trial protocols at the trial centers, Monitor the enrolment of patients,Monitor that all documentation is done in compliance with the protocol e.g. CRF’s,Follow SOPs and GCP regulations and be responsible for acquiring and processing of data generated from the studies,Assistance of the PI at clinical trial site for the assigned clinical trials,Ensure that all the queries are addressed and documented and that revised or final reports are scheduled and mailed,Collect and analyse study data
Requirements-MBBS, MD/MS, M.Pharm, B.Pharm, M.Sc, B.Sc, PG Diploma, Phd, 1-4yrs exp
Contact-United Health Group
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