Clinical Trial Compliance Manager

7 days ago


ghaziabad, India beBeeClinical Full time

Clinical Compliance Specialist Role This position involves ensuring compliance and quality in clinical trials. The job entails conducting audits, reviewing documentation, and verifying adherence to protocols, regulations, and guidelines. Main responsibilities include: Conducting site audits, reviewing CRFs, informed consent forms, and regulatory documents; Identifying and reporting audit findings, recommending corrective actions; SUPPORTING SITE STAFF WITH COMPLIANCE GUIDANCE AND TRAINING; Preparing audit reports and following up on CAPA implementation; The ideal candidate will have a degree in life sciences or related field, 10-12 years of clinical research experience, with auditing and QA experience, knowledge of GCP, ICH guidelines, and FDA/EMA regulations, strong communication, analytical, and organizational skills, and ability to travel.



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