Synova Partners is supporting an extremely well-funded, rapidly growing PFA start-up as they look to scale their European clinical team.
Position Summary
This is a key Clinical Affairs position supporting the delivery of international clinical studies for a growing medical device company. You’ll play a hands‑on role in ensuring trials are executed to the highest standards, working closely with investigators, sites, and cross-functional teams across Europe.
The role is ideally suited to someone based in Europe and within easy reach of a major airport (with a preference for the Netherlands, Italy, the Czech Republic, or Poland), given the level of travel and site interaction involved.
What you’ll be doing
* Acting as a key point of contact for clinical trial sites, building strong relationships with investigators, CROs, and external partners
* Supporting the full lifecycle of studies, from site initiation through to monitoring visits and close‑out
* Collecting and managing clinical and procedural data in line with study protocols and regulatory requirements
* Providing on-site support during cases, ensuring procedures are carried out in line with the protocol and product guidelines
* Assisting with adverse event reporting and ensuring compliance with GCP, ISO 14155, and local regulatory standards
* Helping to troubleshoot clinical or technical challenges in a proactive, solutions‑focused way
* Supporting logistics around devices and clinical supplies, including inventory management and shipments
* Maintaining accurate study documentation and tracking progress using internal systems and tools
What they’re looking for
* Around 3+ years’ experience supporting clinical trials (ideally multi‑site), within medical devices
* Exposure to cardiology or interventional device trials would be a strong advantage
* Comfortable working in hospital and operating room environments, supporting live cases
* Good understanding of clinical trial processes, GCP, and regulatory frameworks
* Strong communication skills and the ability to build credibility with clinical stakeholders
* Highly organised, proactive, and able to operate independently in a fast‑paced environment
* Fluent in English, with additional European languages a plus
This is a highly visible, field‑based role with significant exposure to physicians and cutting‑edge technology, offering the opportunity to be directly involved in bringing new therapies through clinical development.
Travel is a key component of the position (circa 60–85%), so it would suit someone who enjoys being on‑site and working closely with clinical teams.
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