Clinical Data Reviewer – Sponsor-dedicated

• Perform ongoing clinical data review to ensure data quality, consistency, and completeness
• Identify discrepancies and raise/resolve queries in EDC systems
• Review patient data including eligibility, medical history, treatment, safety data, and outcomes
• Contribute to and follow the Data Review Plan (DRP)
• Cross-check data across multiple sources, including EDC, labs, and safety databases
• Support data cleaning activities ahead of interim analyses and database lock
• Collaborate with Clinical, Data Management, and Operations teams to resolve data issues
• Monitor site data entry performance and escalate risks or delays
• Participate in study meetings and provide status updates on data review activities
• Ensure compliance with GCP, protocols, and regulatory requirements

• Scientific background (e.g., MSc, PhD, MD, PharmD, Nursing)
• 8+ years of experience in clinical trials, with strong clinical data review expertise
• Experience with EDC systems, data review tools, and query management
• Strong understanding of clinical trial processes and GCP
• Experience with coding dictionaries (e.g., MedDRA) is a plus
• Excellent attention to detail, communication, and stakeholder collaboration skills
• Equivalent experience, skills, and/or education will also be considered

• Career development and progression
• Supportive and engaged line management
• Technical and therapeutic area training
• Peer recognition
• Total rewards program
• Inclusive culture
• Reasonable accommodations, when appropriate