Clinical Research Associate
Job Description:
The incumbent will be responsible for the following:
ï‚· Perform site feasibility, site selection visit as per protocol and sponsor requirement.
ï‚· Perform site initiation visit to train study personal on protocol, regulatory and sponsor requirements.
ï‚· Perform routine monitoring at sites which would include source data verification, IP accountability, lab data review etc.
ï‚· Coordination with various stake holders eg. IP depo, IVRS, central laboratory, logistics vendors etc for site related activities
ï‚· Off site managements eg. review of e-crf, resolution of queries, maintain and track inhouse TMF, attending internal study meeting etc.
ï‚· Providing site related updates to lead CRA/PM for sponsor meeting.
ï‚· Should have worked on multiple therapeutic area’s
Key Skills :
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