Clinical Data Reviewer (Sponsor-dedicated) - Poland / Spain / UK, remote

Syneos Health® is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress.

Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape. Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you’ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver – for one another, our customers, and, most importantly, for those in need.

We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program. We are committed to building an inclusive culture – where you can authentically be yourself. Central to this is our purpose – Driven to Deliver – which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone’s life.

Job Responsibilities:

• 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 (e.g., EDC, labs, 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

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

Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities. Equivalent experience, skills, and/or education will also be considered so qualifications of incumbents may differ from those listed in the Job Description.