Clinical Scientist
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Job Description
Clinical Scientist supporting design and execution of real-world evidence research studies at Heart Rhythm Clinical Research Solutions. Collaborating with multidisciplinary teams to translate findings into clinical advancements.
Responsibilities:
- The Clinical Scientist supports the design, execution, analysis, and dissemination of real-world evidence and implementation research studies.
- 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
- 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
- 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
- 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
- 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.
Requirements:
- 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
Benefits:
- Occasional domestic travel may be required for company meetings, audits, etc.
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