ppbEblex Group /b is supporting an innovative bbiotechnology company /b in Spain to appoint an experienced bGCP Consultant /b to provide quality oversight across its clinical development programmes. /p pThis is an excellent opportunity to work with a growing biotech, ensuring clinical studies are conducted in compliance with bICH-GCP, EU Clinical Trial Regulation, and EMA requirements /b, while supporting inspection readiness and quality management activities. /p h3Key Responsibilities /h3 ul liProvide GCP quality oversight across Phase I–III clinical trials /li liSupport GCP audits, CAPAs, and quality investigations /li liEnsure compliance with ICH-GCP, EU CTR, and company SOPs /li liReview clinical trial documentation and Trial Master Files (TMFs) /li liPartner with Clinical Operations, Regulatory Affairs, Medical,



and external CROs /li liSupport inspection readiness and continuous quality improvement initiatives /li /ul h3Requirements /h3 ul li5+ years' experience in GCP Quality Assurance or Clinical Quality within biotech, pharma, or CRO environments /li liStrong knowledge of bICH-GCP, EU Clinical Trial Regulation, and EMA guidance /b /li liExperience supporting clinical trials and regulatory inspections /liliPrevious biotech experience preferred /li liFluent English required. Spanish is a plus /li /ul pbEblex Group /b is managing this search exclusively. Apply or contact us for a confidential discussion. /p /p #J-18808-Ljbffr

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