Teva Pharma Job Vacancy For Clinical Research Associate
Job Description
To monitor and do a quality check of all study related activities such as check-in related procedures, dosing, sample collection, processing, segregation, transfer and check-out as described in SOP CL-L065.
Coordinating with project management Group (PMG) for compliance with sponsor requirements and timelines.
Periodic review on status of study files until archival of the files.
Coordinating with PMG and Lab technicians for the dispatch of biological samples to client and analytical department.
Coordinating with Medical writing group for the movement of files to the concerned department and ensuring to maintain timelines.
Coordinating with PMG and investigators in resolving the queries raised by sponsors/
Compilation of study data, SDTM and review clinical reports.
To carry-out other responsibilities as and when assigned by the management.
Coordinating with the Ethics Committee for submission of protocol and other study related documents.
Report to Principal investigator on study related activities.
To report to respective Centre Head on all activities.
Qualifications
MSC/ M.Pharm with 2-5 years of experience
Function
Research & Development
Sub Function
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