Senior Clinical Research Auditor

4 days ago


india beBeeClinicalResearch Full time

Quality Assurance Specialist RoleClinical Site Auditors guarantee adherence to quality and regulatory standards at Clinical Trial sites by conducting site assessments, examining documentation, and confirming compliance with protocols, GCP, GLP, and regulatory requirements.Main Responsibilities:Conduct clinical research site audits across phases I–IV.Review CRFs, informed consent forms, and regulatory documents.Identify and document audit findings; suggest corrective actions.Provide compliance guidance and training to site staff.Prepare and follow up on CAPA implementation reports.Requirements:Bachelor's degree in life sciences, nursing, pharmacy, or related field.10-12 years of experience in clinical research, including auditing and QA.Familiarity with GCP, ICH guidelines, and FDA/EMA regulations.Strong communication, analytical, and organizational skills.Able to travel for site visits.About the Job:This role is responsible for ensuring the highest standards of quality and compliance at Clinical Trial sites. The ideal candidate will have a strong background in clinical research and a keen eye for detail.What We Offer:We offer a competitive compensation package and opportunities for professional growth and development.



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