Clinical Compliance Specialist

1 week ago


india beBeeAuditor Full time

Key Roles:Conduct comprehensive site audits to ensure compliance and quality at clinical trial sites.Review CRFs, informed consent forms, and regulatory documents to identify audit findings.Provide guidance and training to site staff on compliance and protocol adherence.Prepare detailed audit reports and follow up on CAPA implementation.Requirements:10-12 years of experience in clinical research with a focus on auditing and QA.Strong communication, analytical, and organizational skills.Able to travel extensively for site audits.Preferred qualifications include certification in Clinical Research or Quality Auditing (ACRP, SOCRA).Experience with eTMF and EDC systems is also desirable.Working Conditions:Up to 50% travel to clinical sites.Combination of remote and field work.



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