Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s motto is Science with Integrity. Cliantha has fifteen years of impeccable regulatory history with USFDA, WHO, MHRA, Health Canada, AGES, AEMPS, MCC, MOH, ANSM, MOPH, ANVISA, CAP, and NABL.
Post : Report Specialist
Qualification : B.Pharm / M.Pharm / M.Sc
Experience : 2 - 8 Years
Job Description :
A. Prepare Sample analysis report and Method validation report in compliance with standard operating procedure.
B. Ensure report is prepared as per respective regulatory and sponsor requirement.
C. Handle Sponsors or regulatory queries on lab reports.
D. To ensure that lab reports are released within their timelines.
E. Maintain documents and databases for the assigned projects.
F. Compile copies of Method validation report and Sample analysis report for archiving
Job Location : Ahmedabad
Please share CV at dmirchandani@cliantha.com
Last Date : 25th April, 2023
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