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Principal Clinical Research Scientist
Ceribell │ Point-of-Care EEG. Own the full lifecycle of clinical evidence generation from gap analysis through literature review, study conception, protocol development, data collection and analysis, to manuscript authorship and publication in peer-reviewed journals .
Posted 9/17/2026full-timeSunnyvale • California • United StatesLead💰 $168,000 - $185,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical evidence generation, including study design, statistical analysis, and scientific writing, while effectively collaborating with cross-functional teams to ensure regulatory compliance and data integrity.
Highest-signal resume keywords
PhD In Clinical ResearchClinical Research ExperienceStatistical Analysis (R, Python)Scientific WritingClinical Trial Design
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical Evidence GenerationData AnalysisProtocol DevelopmentManuscript AuthorshipLiterature ReviewClinical Data InterpretationPublication ManagementRegulatory SubmissionsStudy DesignData Visualization
Soft Skills
Excellent Communication SkillsRelationship ManagementCollaborationPresentation Skills
Industry Keywords
Medical Device IndustryPharmaceutical IndustryFDA 510(k)Neuroscience ExpertiseKOL EngagementClinical Evidence LibraryPublication PipelineScientific Conferences
Tech Stack
Tools & technologiesPythonGo
About the role
Key responsibilities & impact- Own the full lifecycle of clinical evidence generation from gap analysis through literature review, study conception, protocol development, data collection and analysis, to manuscript authorship and publication in peer-reviewed journals
- Author and present scientific communications, including abstracts, manuscripts, posters, and presentations, for peer-reviewed and commercial audiences at scientific conferences and congresses
- Manage the clinical evidence library and publication pipeline, maintaining timelines and coordinating with Regulatory and Marketing on publication and presentation strategy
- Support regulatory submissions with clinical evidence and clinical trial results, including FDA 510(k)
- Contribute to prospective and retrospective clinical study design for existing and future products
- Interface with study investigators, KOL advisors, and internal Data Science, Regulatory, Marketing, and Product teams
- Maintain relationships with clinical and scientific leaders to advance study execution, analysis, and results dissemination
- Develop and execute conference activities, including abstract/presentation submissions, KOL engagement, and investigator coordination
- Partner with Marketing, Sales, and Go-to-Market teams to develop clinical evidence summaries, infographics, and data visualizations while ensuring scientific integrity, data accuracy, and regulatory compliance
- Perform other responsibilities as assigned by the Manager/Supervisor
Requirements
What you’ll need- PhD in Clinical Research, Engineering, Epidemiology, Biostatistics, Public Health, or related life science discipline
- 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 diverse audiences (clinicians, regulators, commercial teams)
- Preferred: 8+ years of clinical research experience in the medical device industry
- Preferred: Neuroscience expertise
- Preferred: Clinical trial or clinical data study design experience
- Comprehensive list of publications required alongside resume
Benefits
Comp & perks- 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
- Employee Stock Purchase Plan (ESPP) with a discount
- Monthly cell phone stipend
- Flexible paid time off
- 13 Paid Holidays + 3 Company Wellness Days
- Excellent parental leave policy
- Fantastic culture with tremendous career advancement opportunities
- Joining a mission-minded organization!