Job Overview
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Date Posted26/05/2023
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Location (State / UT)
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Expiration date--
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Experience1 Year, 6 Years
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GenderAny
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Desired QualificationMaster’s Degree
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Salary in (₹)Negotiable
Job Description
Role & Responsibilities:
- To undertake Quality control checks for documentation during the clinical phase of the bio study
- To monitor for compliance with study protocol during bio study
- To check the protocol, ICF, CRF, and other documents for a bio study
- To verify the corrective actions taken against observations during the quality audit and to ensure their implementation
- To support the process of enhancing the quality of clinical data
- To check and verify instrument/system-related documentation
- To prepare the SOPs and monitor their periodic updation
Desired Candidate Profile:
- MS/M.Sc(Science) in, M.Pharma.
- 1-5 Years of Relevant Experience