Principal Scientist, Clinical Research – MedTech Surgery

Johnson & Johnson

Principal Scientist leading clinical research and evidence strategies for Johnson & Johnson MedTech’s robotic surgery platform. On-site in Santa Clara or Cincinnati, supporting global trials and regulatory submissions.

Posted 8/21/2026full-timeSanta Clara • California, Ohio • 🇺🇸 United StatesLead💰 $134,000 - $231,150 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research science and processes, with a strong focus on developing and delivering evidence generation strategies for clinical trials. Proven ability to lead cross-functional teams and build relationships with key stakeholders in the healthcare market.

Highest-signal resume keywords

Clinical Research Science ExpertiseRobotics ExperienceGlobal Regulatory SubmissionsClinical Trial DesignEvidence Generation Strategies

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical ResearchEvidence GenerationClinical Trial DesignRegulatory ComplianceProduct Development ProcessesSurgical ResearchData InterpretationBudget ManagementStrategic AssessmentReal-World Evidence

Soft Skills

LeadershipCollaborationRelationship BuildingInfluencingCommunication

Industry Keywords

Medical DevicesBiologicsClinical TrialsHealthcare MarketGlobal Clinical Trial RegulationsSOP ComplianceMarket AccessHealth EconomicsPre-Clinical StudiesPost-Market Approval

About the role

Key responsibilities & impact

Provide scientific leadership for Johnson & Johnson MedTech Surgery's Robotic Surgery Platform
Collaborate with multi-functional evidence teams, including Medical, Clinical, Pre-clinical, and Health Economics and Market Access
Develop and deliver global evidence generation strategies for pre- and post-market approval studies, investigator-initiated studies, and real-world evidence
Ensure input and alignment from strategically important regional MedTech leads
Design clinical trials to meet premarket and post-market needs
Strengthen capability in and drive implementation of real-world evidence
Develop a network with key surgeons in the US, EU, and APAC to assist in execution of Robotic Surgery clinical trials
Lead cross-functional teams to interpret and disseminate evidence, including CSRs, abstracts, and manuscripts
Support clinical scientific discussions with regulatory agencies and notified bodies
Review clinical evidence generated for marketing authorization and line extensions, including during sponsor regulatory inspections
Provide scientific, technical, and strategic assessment of new business development opportunities and support acquisition of innovative products
Influence, shape, and lead teams
Build relationships internally and partnerships with business partners and customers/investigators
Travel domestically up to 25% as required

Requirements

What you’ll need

A minimum of a Bachelor’s degree in Biological Science, Engineering, or a related field is required
A minimum of 8 years of related scientific / technical experience within Clinical Research required
Expertise in clinical research science and processes
Broad and extensive understanding of product development processes, team dynamics, healthcare market environment, clinical trends, and global clinical trial regulations
Proven track record of contributing to clinical programs within a clinical or surgical research setting, on time, within budget, and in compliance with SOPs and US regulations
Experience working in Robotics strongly preferred
Experience supporting global regulatory submissions for medical devices, biologics, or drugs preferred
Up to 25% domestic travel may be required

Benefits

Comp & perks

Retirement plan (pension)
Savings plan (401(k))
Long-term incentive program
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member; 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52-week rolling period
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year
Inclusive interview process and disability accommodations