Clinical Data Reviewer – Sponsor-dedicated

This is a fully remote position, open to applicants in Spain.

📋 Description

• Conduct continuous reviews of clinical data to ensure quality, consistency, and completeness.

• Detect discrepancies and initiate/resolves queries within EDC systems.

• Analyze patient data including eligibility criteria, medical history, treatment details, safety information, and outcomes.

• Contribute to and adhere to the Data Review Plan (DRP).

• Verify data across various sources (e.g., EDC, laboratories, safety databases).

• Assist with data cleaning processes prior to interim analyses and database closure.

• Work collaboratively with Clinical, Data Management, and Operations teams to address data-related challenges.

• Track site data entry performance and report risks or delays.

• Engage in study meetings and deliver updates on data review progress.

• Ensure adherence to GCP, study protocols, and regulatory standards.

⛳️ Requirements

• A scientific background (e.g., MSc, PhD, MD, PharmD, Nursing).

• Over 8 years of experience in clinical trials, demonstrating strong expertise in clinical data review.

• Familiarity with EDC systems, data review tools, and query management.

• A solid grasp of clinical trial processes and GCP guidelines.

• Experience with coding dictionaries (e.g., MedDRA) is advantageous.

• Exceptional attention to detail, communication, and skills in stakeholder collaboration.

🏝️ Benefits

• We are dedicated to the development of our employees through career advancement opportunities.

• Supportive and engaged management.

• Technical training and therapeutic area education.

• Peer recognition and a comprehensive rewards program.

• Committed to fostering an inclusive workplace culture.