Clinical Field Specialist

Our client is developing a novel medical device. It is an exciting time for all who work at the company. With promising early-stage results (to be released in 2026), they are now entering into a European wide Clinical study.

This is an opportunity to join a rapidly growing Medical Device manufacturer and be part of this unique Device study.

You will be the be the ‘go to’ person and cover the implant solo for the company.

Exciting times ahead….what to find out more?

KEY ACCOUNTABILITIES

Site Management & Monitoring

• Conduct qualification, initiation, routine monitoring, and close-out visits in accordance with the monitoring plan.
• Ensure site adherence to the protocol, regulatory requirements, ISO 14155, and SOPs.
• Verify informed consent procedures and patient eligibility checks.
• Perform source data verification (SDV) and ensure timely resolution of queries.
• Provide ongoing training and support to...