Clinical Trial Compliance Specialist

7 days ago


dombivli, India beBeeCompliance Full time

Clinical Quality Compliance Manager Job DescriptionAs a Clinical Site Auditor, you will ensure compliance and quality at Clinical Trial sites. You will conduct site audits, review documentation, and verify adherence to protocols, GCP, GLP, and regulatory requirements.About the Role:This is a key position responsible for ensuring clinical trial sites meet strict regulatory requirements.The successful candidate will be responsible for conducting thorough audits of clinical research sites, reviewing documentation, and verifying compliance with established protocols.Key Responsibilities:Conduct regular audits of clinical research sites across phases I–IV.Review case report forms, informed consent documents, and other regulatory files.Identify and document any non-compliance issues, recommending corrective actions as needed.Provide guidance and training to site staff on compliance procedures.Publish comprehensive audit reports, highlighting areas for improvement and implementing corrective actions.Benefits:This role offers a competitive salary package, opportunities for professional growth and development, and the satisfaction of working in a dynamic healthcare environment.



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