Clinical Research Quality Assurance Professional

1 week ago


kolkata, India beBeeClinical Full time

Clinical Research Compliance SpecialistEnsuring adherence to protocols, regulatory requirements and quality is a key aspect of this role.Key Responsibilities:Conduct site audits across phases I–IV.Review CRFs, informed consent forms and regulatory documents.Identify and report audit findings; recommend corrective actions.Support site staff with compliance guidance and training.Prepare audit reports and follow up on CAPA implementation.This specialist will require a bachelor's degree in life sciences or a related field, along with 10-12 years of clinical research experience including auditing and QA. Knowledge of GCP, ICH guidelines and FDA/EMA regulations is essential for success in this position.Qualifications:Bachelor's degree in life sciences or a related field.10-12 years of clinical research experience.Knowledge of GCP, ICH guidelines and FDA/EMA regulations.



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