Freelance Clinical Research Associate - Medical Devices (Denmark)
Ready to be the heartbeat of medical research? Join our client in this Clinical Research position and assist in turning innovative science into life-changing care!
Proclinical is working alongside a small European CRO who specialize in medical device development. Our client is seeking an experienced Freelance Clinical Research Associate to study start up who will manage site monitoring, protocol compliance, and data integrity for their portfolio of device trials.
What We're Looking For:
- Proven years of independent site monitoring experience, including leading monitoring activities autonomously, managing multiple sites, and owning data quality
- Flexibility - freelance engagement; this role is remote with occasional site visits across Denmark.
- Proficiency - CDISC standards, eCRF systems, and regulatory documentation (ICH-GCP)
- Self-directed - Be able to thrive without constant oversight with ability to prioritize protocol adherence and communicate proactively with sponsors and sites
Strongly Preferred
- Medical device trial independent monitoring experience
Day-to-day Tasks:
- Monitor assigned sites for protocol compliance and safety reporting.
- Review source data, manage monitoring plans, and escalate deviations.
- Liaise between study team, sites, and regulatory bodies.
- Maintain detailed monitoring records and trending reports.
If you are having difficulty in applying or if you have any questions, please contact Elis Jones at e.jones@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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