QA – GCP Officer

About the role

The QA – GCP Officer ensures that all clinical trial activities comply with Good Clinical Practice regulations, guidelines and SOPs. This role is responsible for reviewing protocols, documentation and reports to guarantee regulatory compliance and high‑quality standards.

Key responsibilities

• Review clinical trial protocols and reports to confirm adherence to GCP and regulatory requirements.
• Ensure complete and accurate documentation of study protocols, informed consent forms, trial master files and other trial records.
• Monitor study close‑out, dispensing and clinical conduct procedures, and follow up on any deviations.
• Maintain qualification of the environment and instruments used in bioequivalence and other studies.
• Verify that training and delegation records for participating staff meet study requirements.
• Participate in internal audits of operations and facilities and update quality‑assurance procedures as needed.

Required profile

• B.Sc. in Pharmacy.
• 0–2 years of relevant experience.
• Fluent in Arabic and English, both spoken and written.

Required skills

• Windows operating system.
• Microsoft Excel.
• Microsoft Word.
• Microsoft PowerPoint.