Clinical Data Reviewer – Sponsor-dedicated

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

📋 Description

• Conduct continuous clinical data evaluations to guarantee data quality, consistency, and completeness.

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

• Assess patient information including eligibility, medical history, treatment, safety data, and outcomes.

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

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

• Assist in data cleaning tasks prior to interim analyses and database closure.

• Collaborate with Clinical, Data Management, and Operations teams to address data issues.

• Monitor site data entry performance and report any risks or delays.

• Engage in study meetings and provide updates on data review processes.

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

⛳️ Requirements

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

• Over 8 years of experience in clinical trials, with a strong focus on clinical data review.

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

• A solid understanding of clinical trial processes and GCP.

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

• Exceptional attention to detail, communication, and collaboration skills with stakeholders.

🏝️ Benefits

• Opportunities for career development and advancement.

• Supportive and engaged line management.

• Training in technical and therapeutic areas.

• Recognition from peers.

• Comprehensive total rewards program.