Data Manager for Clinical Trials

Join PSI CRO as a Data Manager for Clinical Trials in this remote full-time position based in Riga, LV, where you'll ensure the integrity and quality of clinical trial data for leading research programmes.

What This Role Involves

As a Data Manager for Clinical Trials at PSI CRO, you'll take ownership of data management operations across multiple clinical research studies. Working remotely from Riga, LV, you'll establish rigorous standards for data collection, validation, and documentation whilst collaborating with clinicians, statisticians, and IT specialists to maintain database integrity and ensure full regulatory compliance.

Day-to-Day Responsibilities

• Design and oversee clinical trial database systems and data management protocols
• Conduct quality assurance reviews and manage data validation to meet regulatory standards
• Monitor and resolve data entry discrepancies across multiple trial sites
• Maintain detailed documentation of data management activities and system changes
• Prepare datasets for statistical analysis in collaboration with trial statisticians
• Ensure adherence to good clinical practice (GCP), GDPR, and PSI CRO standards
• Support clinical trial coordination and reporting from a data management perspective

Qualifications

• Demonstrated experience as a Data Manager in clinical trials or equivalent research data role
• Strong understanding of data management principles, database design, and clinical trial regulations
• Proficiency with clinical trial management systems and database platforms
• Meticulous attention to detail with ability to manage concurrent trials
• Excellent cross-functional communication and team collaboration skills
• Knowledge of good clinical practice (GCP) and data protection regulations (GDPR, HIPAA, or equivalent)

Why Join PSI CRO

PSI CRO provides a dynamic environment where your data management expertise directly shapes the quality and credibility of pharmaceutical and biotech research. Your role in managing clinical trial data means you're contributing to studies that advance patient care and regulatory approvals worldwide. As a remote-based employee in Riga, LV, you'll work alongside an experienced, international team committed to excellence in clinical research operations.

Ready to Apply?

To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.