Clinical Trial Compliance Officer

1 week ago


Tirupati, India beBeeClinicalQuality Full time

Job Title: Clinical Quality Assurance SpecialistClinical Research Sites require meticulous scrutiny to ensure adherence to regulatory requirements, GCP, and GLP standards. As a Clinical Quality Assurance Specialist, you will conduct thorough audits to verify compliance.Audit clinical research sites across phases I–IV to guarantee site quality and data integrity.Conduct in-depth reviews of CRFs, informed consent forms, and regulatory documents.Identify non-compliance issues and provide recommendations for corrective actions.Serve as a key resource for site staff, offering guidance on compliance protocols and providing training sessions.Compile comprehensive audit reports and monitor the implementation of corrective action plans (CAPAs).Responsibilities:In this role, you will be responsible for ensuring that all clinical research sites adhere to established guidelines and regulations, thereby maintaining the highest level of quality and reliability in the data collected.Requirements:Bachelor's degree in a related field or equivalent experience.Strong understanding of GCP, GLP, and regulatory requirements.Excellent communication and analytical skills.Able to work independently and as part of a team.Proficient in MS Office Suite and relevant software applications.Benefits:This is an exceptional opportunity to join our organization and make a significant impact on the quality of clinical research sites. As a valued member of our team, you can expect:A competitive salary and benefits package.Ongoing professional development opportunities.A collaborative and dynamic work environment.



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