
Senior Field Clinical Engineer - EMEA
- Ile-de-France
- CDI
- Temps-plein
- Working under general direction, provides engineering, educational, and technical support in response to field inquiries from physicians and health care professionals involving the company's renal denervation product.
- Performs work that involves a high degree of independence. Identifies and routinely uses the most effective, cost-efficient, and best business practices to execute processes; continually evaluates their effectiveness and appropriateness.
- Exercises independent judgment in planning, organizing, and performing work; monitors performance and reports status to manager.
- Acts as a clinical interface between the medical community and the business.
- Demonstrates ability to build and sustain credible business relationships with customers and shares product expertise accordingly.
- Provides engineering, education, and clinical support in response to field inquiries on an as-needed basis. Demonstrates a thorough command of the TIVUS product, related product and technical knowledge, trends, and players.
- Develops, leads, and/or facilitates trainings and other programs for healthcare professionals.
- Provides insight, guidance, and feedback to management on market feedback and components of next-generation products.
- Provides regional procedural case coverage, potentially across the EMEA region.
- Provides additional back-up support in the following areas:
- Clinical study monitoring/data collection
- Troubleshooting
- New product in-service training to physicians and healthcare professionals
- Continuously develops engineering and technical skills aligned with the company's strategic goals.
- Assists with advanced educational seminars and preparation of educational materials.
- Assists with advanced product demonstrations to visiting physicians and healthcare professionals.
- Remains current on developments in field(s) of expertise, regulatory requirements, and a good working knowledge of company and competitor products, markets, and objectives as well as industry trends.
- Resolves and/or facilitates resolution of problems, including identifying causes to prevent re-occurrence.
- Performs related functions and responsibilities, on occasion, as assigned.
- A Bachelor's degree in Biomedical Engineering, related field, or equivalent healthcare experience.
- A minimum of 5 years of clinical research experience, including coordination of multi-center trials and a solid technical background.
- Fluency in both German and English, written and verbal, to support regional collaboration, training, and communication with internal and external stakeholders.
- Ability and willingness to become certified on the Renal Denervation product.
- Comfortable with extensive travel-up to 75% domestically and within the EMEA region.
- Demonstrated ability to present, write, and teach clinical and medical information effectively.
- Hands-on experience with interventional or catheter-based procedures.
- Strong cross-functional collaboration skills-able to work with engineers, vendors, and customers across various disciplines.
- Proven capability to manage multiple assignments simultaneously while maintaining attention to compliance and detail.
- A proactive approach to identifying and escalating clinical or protocol-related concerns.
- Strong communication skills and fluency in medical terminology.
- Clinical research experience specific to the medical device industry.
- Experience in multi-center cardiology trials.
- Familiarity with GCP and ICH guidelines for regulatory compliance.
- Proficiency in Microsoft Office tools and database management systems.