Cliantha Research, a full-service Clinical Research Organization (CRO), is a leading provider of Clinical research services, based in Ahmedabad, India. Cliantha’s mission 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: Officer / Sr. Officer / Executive / Sr. Executive - QA/QC
Department : QA/QC
Basic qualification required : M.Sc / B.Pharm / M.Pharm
Experience : 1 to 7 Years
A. Conduct In process audit of study activities during clinical phase of the trial.
B. Review Clinical Raw data and Clinical Report for the studies done for pharmaceutical Sponsor in the clinics.
C. Review of Protocol and its attachments.
D. To assure that clinical studies are conducted in accordance to SOPs. compliance to Protocol requirements and guidelines applicable.
E. Review Master Sheet and Randomization.
F. Inspection of Clinics for 6CP Compliances.
G. Review Calibration Documents of clinic instrument.
H. Planning and Conducting of vendor audits, preparation of audit report and ensuring compliances.
Interested candidates can send their resume at firstname.lastname@example.org
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