Clinical Research QA

Responsibilities: Conduct internal audits and ensure audit readiness Implement and manage CAPA processes Ensure compliance with GCP, GLP, and regulatory standards Review SOPs, protocols, and quality documentation Support quality oversight across clinical and laboratory operations Collaborate with logistics teams to ensure compliant sample handling and documentation Train staff on quality systems and compliance requirements Requirements: Degree in Life Sciences, Clinical Research, or related field 2–5+ years QA experience in clinical research or laboratory settings Strong knowledge of GCP, GLP, and regulatory frameworks Experience with audits and CAPA management Logistics/sample chain experience is an advantage