quality_auditor__clinical_trial

Cliantha Research Limited

5 to 7 yrs As per Industry Standards

Ahmedabad (Gujarat)

APPLY Posted on 17 March, 2021

JOB DESCRIPTION

Brief JD A. Plan, conduct and manage Internal & Investigator siteaudits, system audits, vendor audit in compliancewith ICH GCP, protocol, SOP & applicable GxPstandards & regulation.B. Review of deviations and CAPA plans and follow-up toensure compliance.C. Review of SOPs, clinical trial study documents such asprotocol ICD, study plans, clinical study report etc.D. Assist QA manager to facilitate clients/sponsoraudits.E. Candidate must possess strong written and verbalcommunication skills. Strong analytical and problemsolving skills and should able to prioritize work.


FUNCTIONAL AREA :Bio Tech/R&D/Scientist
INDUSTRY :Biotechnology/Pharmaceutical/Medicine, Manufacturing/Industrial
SPECIALIZATION :Clinical Research
ROLE :
QUALIFICATION :Any Graduate

KEY SKILLS

clinical study, ich, clinical, gcp, pharmacology

JOB POSTED BY COMPANY

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