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|
|QUALIFICATION :||Any Graduate|
clinical study, ich, clinical, gcp, pharmacology
JOB POSTED BY COMPANY
To write / check fleejobs review about Cliantha Research Limited, please login.