Clinical Research Compliance Expert

2 weeks ago


ahmedabad, India beBeeQuality Full time

Compliance SpecialistEnsure quality and compliance at clinical trial sites by conducting thorough audits, reviewing documentation, and verifying adherence to protocols, regulatory requirements, and industry standards.Key Responsibilities:Conduct comprehensive site audits across all phases of clinical research.Review case report forms (CRFs), informed consent forms, and relevant regulatory documents.Identify and document audit findings; recommend corrective actions to maintain compliance.Provide guidance and training to site staff on compliance matters.Prepare detailed audit reports and ensure implementation of corrective action plans.Qualifications:Bachelor's degree in a life science or related field.Minimum 10-12 years of experience in clinical research, with a strong background in auditing and quality assurance.Knowledge of Good Clinical Practice (GCP), ICH guidelines, and FDA/EMA regulations is essential.Strong analytical, organizational, and communication skills are required for this role.Able to travel extensively.Attractive compensation packageCompetitive salary range: $80,000 - $110,000 per year, depending on experience. Bonus potential and benefits available.This is an excellent opportunity for a motivated individual to join our team and make a significant contribution to the success of our organization.



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