Clinical Scientist

About Heart Rhythm Clinical Research Solutions

We bring science, data, and collaboration together in a single, full-service CRO model powered by real‑world evidence (RWE).

By combining deep cardiovascular expertise, an engaged and diverse network of physicians, and close client partnerships, we transform data into evidence that fuels innovation and leads to better care.

Our growing network of experts and institutions powers every project we deliver — enabling collaboration, scalability, and measurable results.

270+

Cardiovascular Specialists

100+

Signed Data Sharing Agreements

3+

4

Countries represented

About the role

The Clinical Scientist supports the design, execution, analysis, and dissemination of real‑world evidence and implementation research studies. This role sits at the intersection of clinical research, implementation science, and collaborative medical writing. This role brings a passion for translating scientific insights into clinical and procedural advancement through rigorous methods and cross‑functional teamwork.

The Clinical Scientist contributes to investigator‑initiated and sponsor‑supported research projects, with a strong focus on registry‑based studies, healthcare technology evaluation, and workflow optimization across diverse healthcare settings. This is a core team member in research protocol development, data interpretation, stakeholder engagement, and scientific dissemination.

What you'll do

Scientific Writing & Dissemination

• Lead & support development of scientific manuscripts, white papers, & reports based on HRCRS registry data and partner‑sponsored studies
• Draft abstracts, posters, and oral presentations for national and international scientific meetings
• Translate technical findings into usable outputs for sponsors, investigators, and health system leaders

Collaborative and Team Science

• Contribute to multi‑stakeholder research initiatives, including coordination with clinicians, statisticians, project managers, and device sponsors
• Facilitate and synthesize outputs from collaborative workshops, clinical roundtables, and working groups
• Support and co‑lead implementation planning sessions with external research and clinical teams

Clinical & Implementation Research Support

• Assist with protocol development, study design, and implementation strategies for real‑world studies
• Apply implementation science frameworks to analyze procedural workflows, clinical adoption, and stakeholder feedback
• Generate synthesis reports and decision memos to inform product launches or technology deployment strategies

Data Interpretation & Stakeholder Communication

• Review and interpret results from statistical analyses in collaboration with data teams
• Conduct qualitative or mixed‑methods synthesis of clinician interviews or surveys
• Communicate findings clearly to internal and external stakeholders for actionability and uptake

Quality Improvement and Innovation

• Contribute to internal initiatives to improve scientific deliverables, project workflows, and knowledge translation
• Stay current on trends in implementation research, registry science, and medical device evaluation

Qualifications

• PhD, DrPH, ScD, MD, PharmD, or equivalent terminal degree in Public Health, Epidemiology, Health Services Research, Implementation Science, or a clinical field
• 3+ years of experience in outcomes research, implementation research, health services research, or medical device evaluation (industry or academic setting)
• Demonstrated expertise in writing and publishing scientific manuscripts, abstracts, and regulatory submissions
• Experience collaborating with multidisciplinary research teams, including clinicians, statisticians, and project managers
• Exceptional scientific writing and communication skills for both technical and non‑technical audiences
• Understanding of real‑world evidence generation, including use of registry and observational data
• Familiarity with implementation science frameworks (e.g., CFIR, RE‑AIM) and dissemination strategies
• Proficiency in collaborative platforms and team science tools (e.g., Google Workspace, MS Teams, version control tools, project tracking software)
• Ability to translate complex data and stakeholder feedback into clear recommendations and reports
• Flexible, detail‑oriented, and comfortable working in fast‑paced, high‑accountability environments

LOCATION AND TRAVEL REQUIREMENTS

This is a fully remote position and may be performed anywhere within the United States of America. Occasional domestic travel may be required for company meetings, audits, etc.

This employer participates in E‑Verify and will provide the federal government with your Form I‑9 information to confirm that you are authorized to work in the U.S.