Teva is a global pharmaceutical leader and the worlds largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day.
Post : Clinical Research Assoc I
Job Description
• To monitor and do a Quality Check of all study activities such as check-in related procedures, dosing, sample collection, processing, segregation, transfer and check-out.
• Co-ordinating with Project Management Group (PMG) for compliance with the sponsor requirements and timelines.
• Periodic review on status of study files up to archival of files.
• Co-ordinating with PMG and lab technicians for the dispatch of biological samples to client and analytical department.
• Co-ordinating with Medical Writing Group for the movement of files to the concerned department and ensuring to maintain timelines.
• Co-ordinating with PMG and Investigators in resolving the queries raised by the sponsors.
• Compilation of study data, SDTM and review of 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.
Additional Information
Experience : 0-4 years
Qualification : M.Pharma/ M.Sc
Location : Bangalore, IN
Industry Type : Pharma
Functional Area : Research & Development
End Date : 30th June, 2022
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