Freelance CRA

Overview
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's degree in a related field, advanced degree preferred
Experience in the neurodegenerative or cardiovascular therapeutic area is a plus
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Research, Analyst, and Information Technology
Industries
Hospitals and Health Care
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