Remote Clinical Data Reviewer – Trial Data Quality Pro

3015 Syneos Health Poland sp. z o.o.; Poland; Remote; PLN 180,000 - 280,000; Full time

Job summary

Syneos Health, a leading life sciences services organization, is hiring a Clinical Data Reviewer (Sponsor-dedicated) for Poland / Spain / UK, with remote options. The role focuses on ongoing data review to ensure data quality, identify discrepancies, and support DRP execution across EDC systems and trials.

Candidates should have a strong scientific background and 8+ years in clinical trials, with experience in data review, MedDRA, and cross-functional collaboration to drive data integrity and

Qualifications

• 8+ years of experience in clinical trials and data review.
• Experience with EDC systems and query management.
• Knowledge of MedDRA is a plus.
• Excellent attention to detail and stakeholder collaboration skills.

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, history, treatment, safety data and outcomes.
• Contribute to Data Review Plan (DRP) and cross-check data across sources.
• Support data cleaning ahead of interim analyses and database locks.
• Collaborate with Clinical, Data Management and Operations to resolve issues.
• Monitor site data entry performance and escalate risks or delays.
• Provide status updates in study meetings and during data review activities.
• Ensure compliance with GCP and regulatory requirements.

Skills

EDC systems

Data review

GCP knowledge

Communication

Education

MSc/PhD/MD/PharmD/Nursing

Tools

MedDRA

Job description

Syneos Health, a leading life sciences services organization, is hiring a Clinical Data Reviewer (Sponsor-dedicated) for Poland / Spain / UK, with remote options. The role focuses on ongoing data review to ensure data quality, identify discrepancies, and support DRP execution across EDC systems and trials.

Candidates should have a strong scientific background and 8+ years in clinical trials, with experience in data review, MedDRA, and cross-functional collaboration to drive data integrity and