Help us change the way the world detects and manages cardiovascular disease

FibriCheck is a fast-growing digital health and MedTech company on a mission to prevent strokes and improve cardiac care worldwide. Our FDA-cleared and CE-marked AI-powered Software as a Medical Device (SaMD) enables people to detect and monitor cardiovascular conditions using everyday devices such as smartphones.

We empower patients with actionable health insights, support clinicians with meaningful clinical data, and help healthcare systems deliver proactive, cost-efficient care. Through partnerships with hospitals, health systems, insurers, wearable manufacturers, and digital health platforms, FibriCheck is redefining how heart health is managed—remotely, digitally, and at scale.

Headquartered in Belgium with a rapidly expanding presence in the United States, we are seeking a US-based Clinical Implementation & Research Specialist to support clinical deployments, research initiatives, and ongoing partner success across the US and international markets.

About the role

As a Clinical Implementation & Research Specialist, you will serve as a key clinical liaison between FibriCheck, healthcare partners, and research collaborators. Based in the US, you will lead and support clinical implementations and research activities for US (and international) partners, while collaborating closely with international teams and supporting global initiatives.

This role combines clinical expertise, project management, and customer-facing communication. You will ensure successful onboarding and adoption, support clinical research execution, and contribute to high-quality clinical and regulatory documentation across markets.

Key responsibilities

• Clinical implementation & customer success (primary US focus)
• Lead clinical onboarding and implementation for US healthcare systems, provider groups, and commercial partners.
• Act as the primary clinical point of contact during implementation, go-live, and post-launch support phases.
• Train clinicians, care teams, and partner stakeholders on clinical workflows, product usage, and best practices.
• Identify and resolve clinical, operational, or workflow-related challenges to drive adoption and long-term success.
• Monitor clinical usage and performance metrics and proactively recommend optimization strategies.
• Provide structured feedback from the field to product, commercial, and medical affairs teams.
• Support sites in configuring RPM/CCM workflows, documentation, and reporting requirements in collaboration with billing stakeholders and partners.

Clinical research support

• Support the planning, setup, and execution of clinical research studies, including feasibility assessments, site onboarding, investigator training, and operational coordination.
• Collaborate with US and international research partners, academic institutions, and CROs as needed.
• Ensure studies are conducted in accordance with applicable regulatory, ethical, and quality requirements.
• Translate clinical and research findings into actionable insights for internal stakeholders.

Clinical and regulatory contribution

• Contribute to the development and maintenance of clinical documentation, including clinical evaluations, literature reviews, post-market clinical follow-up, and regulatory submissions.
• Support alignment between US and international clinical and regulatory expectations (e.g., FDA and EU MDR).
• Provide clinical input to support audits, inspections, and partner inquiries when required.

Qualifications

• 3–5+ years of experience in a clinical-facing role such as Clinical Specialist, Clinical Application Specialist, Research Coordinator, Implementation Manager, or similar within MedTech, Digital Health, or SaaS. Prior experience in cardiology is a plus.
• Bachelor’s or Master’s degree in life sciences, biomedical sciences, nursing, public health, or a related field.
• Experience working with US healthcare systems, clinical implementations, or clinical research environments.
• Strong understanding of clinical workflows and the ability to translate clinical needs into practical solutions.
• Excellent communication and presentation skills, with comfort engaging clinicians, researchers, and executive stakeholders.
• Strong organizational and project management skills; ability to manage multiple implementations or studies in parallel.
• Familiarity with clinical research methodologies and evidence generation is a strong plus.
• Fluency in English is required; additional languages are a plus but not required.
• Willingness to travel domestically and internationally (including Europe) up to ~50%.

What we offer

• A high-impact, customer-facing clinical role in a mission-driven digital health company.
• Direct involvement in scaling US clinical implementations while contributing to global clinical and research initiatives.
• Exposure to both FDA and EU MDR clinical and regulatory environments.
• Flexible, hybrid working model with autonomy and competitive compensation.
• The opportunity to grow into a key clinical reference role as FibriCheck expands in the US.

If you’re energized by our mission and excited to help shape the future of digital cardiovascular care, we’d love to hear from you.

Please send your resume and a brief motivation to career@fibricheck.com.