Senior Clinical Research Associate (CRA)

Role Description

We are seeking a Senior Clinical Research Associate to monitor and coordinate phase II and III clinical trials at Baltic hospital sites, ensuring absolute GCP compliance.

Requirements & Scope

• University degree in Pharmacy, Medicine, or Life Sciences.
• 3+ years of active site-monitoring experience as a CRA.
• Strong knowledge of ICH-GCP guidelines and clinical trials regulations.
• Willingness to travel locally across the Baltic states.

Perks & Benefits

• Dedicated travel allowances and per diems.
• Comprehensive wellness and sports memberships.
• State-of-the-art home office tech stack.
• Continuous medical training certifications.