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Principal Clinical Scientist
Danaher CorporationPrincipal Clinical Scientist designing clinical studies and regulatory strategies for Danaher Diagnostics. Collaborating with multiple teams and liaising with regulatory bodies for product approvals and commercialization.
Posted 7/21/2026full-timeChaska • Florida, Minnesota • 🇺🇸 United StatesLead💰 $120,000 - $165,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical study design and methodology, with a strong focus on regulatory submissions and cross-functional collaboration. Proven ability to mentor junior scientists and effectively communicate with regulatory bodies and internal teams.
Highest-signal resume keywords
Clinical Study DesignRegulatory SubmissionsCross-Functional CollaborationClinical Research ExperienceCommunication Skills
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical ResearchStudy MethodologyRegulatory DocumentationEvidence StrategiesProblem Solving
Soft Skills
Interpersonal SkillsMentoring
Industry Keywords
Life SciencesHealthcareDiagnosticsMedical DevicePharmaceutical IndustryUS TrialsEU Trials
About the role
Key responsibilities & impact- Design clinical studies and evidence strategies supporting global regulatory submissions
- Act as a scientific and clinical liaison with regulatory bodies and external sites
- Partner cross-functionally with R&D, Regulatory, Medical Affairs, Quality, and Commercial teams
- Author and review clinical and regulatory documentation to support product clearance and commercialization
- Build strong internal and external collaborations and mentor junior scientists
Requirements
What you’ll need- Bachelor’s degree in Life Sciences, Healthcare, or a related field with 9+ years of experience in clinical research
- Significant experience in US and/or EU trials
- In-depth understanding of clinical study design and methodology in diagnostics, medical device, or pharmaceutical industry
- Ability to identify and solve complex issues in clinical trial conduct
- Excellent communication (written and verbal) and interpersonal skills
Benefits
Comp & perks- Health insurance
- 401(k) retirement plan
- Paid time off
- Flexible work arrangements
- Professional development opportunities
- Bonus/incentive pay