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
Key Skills & Competencies
- 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.