Clinical Quality Oversight Specialist (6‑month contract)

About the role

Our pharmaceutical client is looking for a Clinical Quality Oversight Specialist on a 6‑month fixed‑term contract. The role will be based in Greater Paris and requires three days per week on site. You will be responsible for ensuring quality compliance across clinical activities, both internal and external, and for supporting the management of investigational medicinal products (IMP) throughout their lifecycle.

Key responsibilities

• Qualify and provide lifecycle oversight of subcontractors selected for clinical operations under Good Clinical Practice (GCP) standards.
• Oversee IMP manufacturing processes in accordance with Good Manufacturing Practice (GMP) and manage the end‑to‑end supply chain.
• Act as the single point of contact for Clinical Operations, Manufacturing, Regulatory Affairs, and Global Quality teams.
• Support external audits, regulatory inspections, and manage quality events.
• Ensure data integrity and adherence to compliance principles.

Required profile

• Experience in clinical quality assurance within the pharmaceutical industry.
• Familiarity with GCP and GMP regulations.
• Ability to coordinate across multiple functional areas and manage external partners.
• Strong understanding of IMP handling and supply chain considerations.

Required skills

• Good Clinical Practice (GCP)
• Good Manufacturing Practice (GMP)
• Investigational Medicinal Product (IMP) oversight
• Data integrity and compliance management