FibriCheck is a fast-growing medtech scale-up on a mission to prevent strokes and improve cardiac care worldwide. Our certified AI-powered Software as a Medical Device (SaMD) solution allows people to detect and monitor cardiovascular diseases anytime and anywhere on everyday devices like a smartphone.
We empower patients and consumers with actionable health insights, support healthcare providers with better data, and help healthcare systems deliver more proactive, cost-efficient care. With partnerships across hospitals, insurers, wearable manufacturers and telehealth platforms, FibriCheck is transforming how heart health is managed: digitally, remotely, and at scale.
Headquartered in Belgium and expanding rapidly with a strong focus on the US, we are now looking for a proactive Clinical Research & Implementation Specialist to be the vital link between our technology and clinical practice.
You are the “boots on the ground” clinical and research expert. Your focus is threefold: (1) ensuring successful medical implementations, (2) coordinating internal and external clinical studies, and (3) maintaining and improving clinical regulatory documentation. You will translate commercial agreements into measurable clinical impact, ensuring our partners (hospitals, researchers, wearable providers, etc.) achieve their goals while maintaining scientific rigor.
- Manage the end-to-end setup for hospitals and clinical partners, ensuring smooth workflow integration and high adoption.
- Leverage your scientific and communication skills to train healthcare professionals, optimize their clinical pathways, and troubleshoot operational issues.
- Translate operational field insights into actionable input for product, commercial, and medical affairs to shape market strategy and product improvements.
- Monitor usage and performance metrics to proactively intervene and ensure long-term value for the partner.
- Oversee and manage the setup and execution of clinical studies, ensuring feasibility, proper investigator training, efficient workflows, and troubleshoot operational issues.
- Support internal and external research initiatives, ensuring compliance with local requirements.
- Translate research insights into actionable input for product, commercial, and medical affairs to shape market strategy and product improvements.
- Actively maintain and improve clinical regulatory documentation ensuring all activities remain compliant, including but not limited to clinical evaluation, literature search, post-market surveillance, and regulatory submissions
- Translate regulatory field insights into actionable input for product, commercial, and medical affairs to shape market strategy and product improvements.
- 3-5+ years in a customer-facing role (e.g., clinical application specialist, research coordinator, implementation manager) within MedTech, SaaS, or Digital Health. Prior experience in cardiology is a plus.
- Bachelor’s or Master’s degree in life sciences, biomedical sciences, nursing, or related field.
- You are analytical, organized, and bring strong project management skills, enabling you to manage timelines and coordinate multiple projects & stakeholders.
- You are a clear and effective communicator who can quantify value and articulate complex scientific concepts in a structured and accessible way.
- Familiarity with clinical evaluations and research methodologies is highly valued.
- Fluent in Dutch and English. Proficiency in German or French is a strong asset.
- Willingness to travel internationally (EU & US) up to ~30%.
- A direct and customer-facing role in a mission-driven company reducing the burden of cardiovascular disease.
- A dynamic environment where you can develop expertise in US/EU market access and clinical innovation.
- Hybrid working model with autonomy and a competitive package.
Energized by our mission and can’t wait to use your first-class talent? Send your resume and a brief motivation to [email protected]. If you are energized by our mission but don’t check every single box, we still encourage you to apply.
