Principal Clinical Research Scientist

Johnson & Johnson

Principal Clinical Research Scientist leading ophthalmic clinical programs for Johnson & Johnson Vision. Driving evidence generation, regulatory strategy, and development of personalized vision-care products.

Posted 8/12/2026full-timeJacksonville • California, Florida • 🇺🇸 United StatesLead💰 $117,000 - $201,250 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in ophthalmic clinical research, including study design, regulatory compliance, and technical writing. Proven ability to lead cross-functional teams and engage with regulatory agencies while delivering clinical programs effectively.

Highest-signal resume keywords

Ophthalmic Clinical Research ExperienceClinical Study DesignTechnical WritingRegulatory ComplianceLeadership on Cross-Functional Projects

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study ProtocolsStatistical Analysis PlansEndpoint StrategyClinical Study ReportsEvidence ReviewClinical PlansMDR-Related DocumentsBiostatisticsOphthalmic DevicesVision Science

Soft Skills

Influencing Without AuthorityCollaborationRelationship Building

Tools & Technologies

ComputersSoftware Programs

Certifications & Qualifications

Advanced Degree in Scientific DisciplineOD, MD/Ophthalmologist, or PhD in Vision Science

Industry Keywords

Clinical OperationsProject ManagementGlobal Strategic MarketingMedical AffairsRegulatory AffairsR&DClinical ProgramsMarketing AuthorizationRegulatory InspectionsProfessional Societies

About the role

Key responsibilities & impact

Represent Clinical Science as a core team member on critical projects
Liaise between project and functional teams and coordinate with Clinical Operations and Project Management partners
Deliver clinical programs on time, within budget, and in compliance with regulations and SOPs
Build collaborative relationships across business platforms and with cross-functional partners including Global Strategic Marketing, Medical Affairs, Regulatory Affairs, and R&D
Lead interpretation and dissemination of evidence through Clinical Study Reports, abstracts, manuscripts, and MDR-related documents such as CERs, PMCFs, and Clinical Plans
Contribute to clinical scientific discussions with regulatory agencies supporting clinical and regulatory strategy
Support proposed investigations, evidence review for marketing authorization, and regulatory inspections
Engage and collaborate with key opinion leaders and regulatory agencies
Build relationships through professional and technical societies
Perform other related duties as assigned by management

Requirements

What you’ll need

Advanced degree in a scientific discipline required
OD, MD/Ophthalmologist, or PhD in Vision Science/related field strongly preferred
5+ years of ophthalmic clinical research experience
Deep understanding of eye care, ophthalmic devices, vision science, or related therapeutic areas
Experience supporting product development and lifecycle management
Led clinical studies or clinical programs, not just participated in them
Experience designing studies and selecting endpoints
Demonstrated leadership on complex, cross-functional projects
Personally authored or substantially contributed to clinical study protocols, Clinical Study Reports, scientific abstracts, and manuscripts/publications
Ability to interpret study results independently
Comfortable working with biostatisticians on sample size assumptions, endpoint strategy, statistical analysis plans, and interpretation of results
Demonstrated ability to influence without direct authority
Experience partnering with R&D, Regulatory Affairs, Marketing, Medical Affairs, and Clinical Operations
Strong technical writing ability required
Understanding of biostatistics as applied to study data required
Proficient with computers and software programs required
Up to 10% domestic or international travel required

Benefits

Comp & perks

Hybrid work arrangement
Retirement plan (pension)
Savings plan (401(k))
Eligibility for the company’s 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
10 days Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year
Inclusive interview process and accommodations for applicants with disabilities