Synova Partners is supporting an extremely well-funded, rapidly growing PFA start-up as they look to scale their European clinical team.
La experiencia que se espera de los solicitantes, así como las habilidades y cualificaciones adicionales necesarias para este trabajo, se enumeran a continuación.
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. xpzdshu
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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