Clinical Specialist

Established Search; Strasbourg; Hybride; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A leading medical technology firm is seeking an EU Clinical Field Engineer to support clinical evaluations and drive procedural excellence in the neurovascular sector across Europe. Candidates should have over 5 years in a clinical role and be fluent in French. This position offers hands-on experience, competitive compensation, and the opportunity to innovate in patient care.

Prestations

Competitive compensation

Growth opportunities

Direct involvement in clinical procedures

Qualifications

• At least 5 years of experience in a clinical‑facing role within the medical device sector.
• Hands-on experience with pre‑market clinical trials in Europe.
• Previous Neurovascular catheter experience.

Responsabilités

• Assist in planning, designing, and managing clinical investigations.
• Deliver hands-on procedural support during live interventions.
• Develop and implement training programs for clinical trial sites.

Connaissances

Clinical methodologies

Medical device technologies

Procedural workflows

Communication with clinicians

Proactive attitude

Fluency in French

Description du poste

Our client a fast-growing, innovation-driven medical device company is seeking an EU Clinical Field Engineer to join its European clinical team. This position plays a critical role in supporting the launch and ongoing evaluation of cutting‑edge devices used in interventional procedures, particularly in neurovascular applications.

Role Overview

In this role, you will be instrumental in coordinating clinical activities before and after regulatory approval. You’ll work closely with healthcare professionals, contribute to clinical strategy, support live procedures, and help ensure regulatory and scientific excellence in every phase of product evaluation and implementation.

Core Responsibilities

• Assist in planning, designing, and managing clinical investigations from early feasibility through post‑market phases.
• Deliver hands‑on procedural support during live interventions, ensuring optimal product performance and procedural efficiency.
• Develop and implement structured training programs and educational resources for clinical trial sites and participating physicians.
• Provide clinical and technical instruction on product usage and trial protocols across European centers.
• Collaborate with product development teams by gathering real‑world clinical insights and supporting technical documentation for regulatory submissions.
• Compile clinical findings into reports and support the preparation of scientific manuscripts and presentations.
• Contribute to post‑market activities such as safety monitoring, adverse event analysis, and clinical evaluations.
• Maintain strict adherence to applicable regulatory guidelines and clinical research standards.
• Foster relationships with clinical leaders and institutions to promote collaboration and feedback loops.
• Track and interpret clinical data trends to inform product refinements and development strategies.
• Stay engaged with the medical community through conferences, training events, and scientific meetings.

Ideal Candidate Profile

• At least 5 years of experience in a clinical‑facing role within the medical device sector, ideally involving minimally invasive or neurovascular technologies.
• Hands‑on experience with pre‑market clinical trials in Europe and working knowledge of relevant regulations.
• Previous Neurovascular catheter experience.
• Strong command of clinical methodologies, medical device technologies, and procedural workflows.
• Independent, proactive, and able to thrive in a fast‑paced, matrixed environment.
• Confident communicating with both clinicians and engineers at a high level.
• Able and willing to travel extensively across Europe, (4 days per week)

Preferred

• Experience in clinical study oversight and medical safety monitoring.
• Fluency in French is required.

Why Join Us?

• Direct involvement in clinical procedures that shape the future of patient care.
• A chance to work with a high‑impact team developing breakthrough medical technologies.
• Growth opportunities in a globally connected, purpose‑driven environment.
• Competitive compensation and a culture that values innovation, quality, and collaboration.