Principal Clinical Research Scientist (Hybrid)

📋 Description

• Own the full lifecycle of clinical evidence generation from gap analysis through literature review
• Author and present scientific communications (abstracts, manuscripts, posters, presentations) for
• Manage the clinical evidence library and publication pipeline, maintaining timelines and
• Support regulatory submissions with clinical evidence and results from clinical trials (e.g., FDA
• Contribute to the design of prospective and retrospective clinical studies on existing and future
• Maintain strong relationships with clinical and scientific leaders (site investigators, principal

🎯 Requirements

• PhD in Clinical Research, Engineering, Epidemiology, Biostatistics, Public Health, or related life
• 5+ years of clinical research experience in the medical device or pharmaceutical industry
• Proficiency in statistical analysis (R, Python, or equivalent)
• Strong scientific writing and experience writing peer-reviewed journal articles
• Demonstrated ability to analyze and interpret clinical data
• Excellent written and verbal communication skills; ability to translate complex clinical data for

🎁 Benefits

• Performance-based incentive compensation (varies by role)
• Equity opportunities
• 100% Employer paid Health Benefits for Employees
• 50% - 70% Employer paid Health, Dental & Vision for dependents (depending on plan selection)
• 100% paid Life and Long-Term Disability Insurance
• 401(k) with a generous company match