Clinical Specialist

Established Search; Paris; À distance; EUR 60 000 - 80 000; Plein temps

Résumé du poste

A leading medical device company in France is seeking an EU Clinical Field Engineer to coordinate clinical activities and support the launch and evaluation of innovative devices in neurovascular applications. The ideal candidate has over 5 years of clinical experience, especially in minimally invasive technologies, and is fluent in French. This role includes extensive travel across Europe and offers a chance to work with breakthrough medical technologies and a high-impact team.

Prestations

Competitive compensation

Growth opportunities

Culture promoting innovation and collaboration

Qualifications

• 5+ years experience in a clinical-facing role in medical devices.
• Hands-on experience with pre-market clinical trials in Europe.
• Confident communicating at high levels with clinicians and engineers.

Responsabilités

• Coordinate clinical activities for product evaluation post-regulatory approval.
• Deliver hands-on procedural support during live interventions.
• Develop training programs and educational resources for clinical trial sites.

Connaissances

Clinical methodologies

Communication with clinicians and engineers

Hands-on procedural support

Data trend interpretation

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.