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Clinical Scientist

Location

Alabama

Posted

70 days ago

Salary

0

Seniority

Senior

Postgraduate Degree3 yrs expEnglish

Job Description

Clinical Scientist

CRS

• 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.

Job 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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