Post : Clinical Research Associate
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, as described in SOP
• 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 Report 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 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.
• Must have strong communication and verbal skills in English
• Must possess strong influential skills and affirmative communication/interpersonal skills
Additional Information
Qualification : M.Pharm
Location : Bangalore
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : R&D
End Date : 05th March, 2019
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