Freelance CRA

Company Description

CRU Global combines world-class clinical operations with strategic investment expertise to de-risk and accelerate the journey of biotech and medtech innovators. Our full-service clinical operations span from preclinical to Phase II/III, with a global network ensuring seamless execution across therapeutic areas. CRU Global has successfully completed over 350 clinical trials and takes pride in advancing scientific research. Our strategic co-investment model through CRU Ventures and PMK Ventures minimizes financial risks and strengthens investor confidence. Operating across Europe, North America, and Asia, we partner with startups, spin-offs, and established players to foster growth at every development stage.

Role Description

This is a Freelance Position for a Clinical Research Associate (CRA) based in the local country. The CRA will be responsible for monitoring clinical trials within the local country.

Experience

• Regulatory submissions know-how
• 5+ years of local monitoring
• Medtech, pharma, and biologics background
• Strong early-phase clinical trials
• Solid ICH-GCP and local guidelines expertise
• Bachelor&aposs degree in a related field, advanced degree preferred
• Experience in the neurodegerative or cardiovascular tehrapeutic area is a plus