Eblex Group is supporting an innovative biotechnology company in Spain to appoint an experienced GCP Consultant to provide quality oversight across its clinical development programmes.

Usted podría ser el solicitante perfecto para este trabajo. Lea toda la información asociada y asegúrese de presentar su candidatura.

This is an excellent opportunity to work with a growing biotech, ensuring clinical studies are conducted in compliance with ICH-GCP, EU Clinical Trial Regulation, and EMA requirements, while supporting inspection readiness and quality management activities.

Key Responsibilities

- - Provide GCP quality oversight across Phase I–III clinical trials

- Support GCP audits, CAPAs, and quality investigations

- Ensure compliance with ICH-GCP, EU CTR, and company SOPs

- Review clinical trial documentation and Trial Master Files (TMFs)





- Partner with Clinical Operations, Regulatory Affairs, Medical, and external CROs

- Support inspection readiness and continuous quality improvement initiatives

Requirements

- - 5+ years' experience in GCP Quality Assurance or Clinical Quality within biotech, pharma, or CRO environments

- Strong knowledge of ICH-GCP, EU Clinical Trial Regulation, and EMA guidance

- Experience supporting clinical trials and regulatory inspections

- Previous biotech experience preferred

- Fluent English required. Spanish is a plus

Eblex Group is managing this search exclusively. xqbhyrx Apply or contact us for a confidential discussion.

📌 Clinical Quality Consultant (Madrid)
🏢 Eblex Group
📍 Madrid