Principal Clinical Research Scientist

Posted 6 Days Ago
Be an Early Applicant
3 Locations
In-Office
117K-231K Annually
Senior level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
Lead clinical research strategy and execution for ophthalmic and vision device programs. Serve as scientific lead, design studies, author clinical documentation, collaborate cross-functionally, engage KOLs and regulators, and manage teams to deliver compliant evidence supporting product development and lifecycle.
Summary Generated by Built In

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.  We provide an inclusive work environment where each person is considered as an individual.  At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Discovery & Pre-Clinical/Clinical Development

Job Sub Function:

Clinical Development & Research – Non-MD

Job Category:

Scientific/Technology

All Job Posting Locations:

Irvine, California, United States of America, Jacksonville, Florida, United States of America, Milpitas, California, United States of America

Job Description:

JOB POSITION SUMMARY

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of vision treatments? Ready to join a team that’s reimagining how vision is improved? Our Vision team solves the toughest health challenges. Help combine cutting-edge insights, science, technology, and people to encourage eye care professionals and patients to proactively protect, correct and enhance healthy sight for life. Our products and services address these needs – from the pediatric to aging eye – in a patient’s lifetime. Your unique talents will help patients on their journey to wellness. Learn more at https://www.jnj.com/medtech

We are searching for the best talent to join our Vision team, as Principal Clinical Research Scientist , J&J Vision, located preferably in Jacksonville, FL, Milpitas, CA, or Irvine, CA.

Purpose:

The Principal Clinical Research Scientist for Vision is an expert in ophthalmic and medical device research who serves as a core team member on key projects and leads a team of Staff Clinical Scientist. This role provides strategic and scientific leadership for the development and execution of clinical programs that generate robust evidence to support innovative vision care products and technologies. Leveraging deep expertise in clinical research, product development, and ophthalmic regulations, the Principal Clinical Research Scientist influences development strategies, aligns cross-functional stakeholders, and drives successful execution of complex initiatives that improve outcomes for eye care professionals and their patients.

You will be responsible for:

Represent Clinical Science as core team member on critical projects, liaising

between project and functional teams, and coordinating with Clinical Operations

and Project Management partners to deliver on time, within budget, and in

compliance with regulations and SOPs.

Activate and build collaborative relationships with across business platforms as well as key cross-functional partners (e.g., Global Strategic Marketing, Medical Affairs, Regulatory Affairs, R&D, etc.) to ensure consistent alignment in new product development and through product life cycle.

Lead initiatives for appropriate interpretation and dissemination of all evidence generated, including Clinical Study Reports, abstracts, manuscripts, and MDR-related documents (CER, PMCF, Clinical Plans, etc.).

Contribute to clinical scientific discussions with regulatory agencies that support the clinical and regulatory strategy, including proposed investigations, review process of evidence to support marketing authorization, and support of regulatory inspections

Engage and collaborate with industry's key opinion leaders, including KOLs and regulatory agencies, and build on relationships established through professional/technical societies

Performs other related duties as assigned by management.  

Qualifications / Requirements:

Education

  • Advanced degree in scientific discipline (required)□

  • OD, MD/Ophthalmologist, or PhD in Vision Science/related field strongly preferred

  • Post-graduate training, residency, or fellowship preferred

Ophthalmic Expertise

  • 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

Clinical Research Leadership

  • Led clinical studies or clinical programs, not just participated in them

  • Experience designing studies and selecting endpoints

  • Demonstrated leadership on complex, cross-functional projects

Technical Writing

□ Personally authored or substantially contributed to:

  • Clinical study protocols

  • Clinical Study Reports (CSRs)

  • Scientific abstracts

  • Manuscripts/publications

Scientific & Statistical Acumen

  • Can interpret study results independently□

  • Comfortable working with biostatisticians on:

  • Sample size assumptions

  • Endpoint strategy

  • Statistical analysis plans

  • Interpretation of results

Communication & Influence

  • Demonstrated ability to influence without direct authority

  • Experience partnering with R&D, Regulatory Affairs, Marketing, Medical Affairs, and Clinical Operations


REQUIRED KNOWLEDGE, SKILLS, ABILITIES, CERTIFICATIONS/LICENSES AND AFFILIATIONS

  • Strong technical writing ability, such as clinical study protocols, reports and abstracts is required

  • Understanding of biostatistics as applied to study data is required

  •  Proficient with computers and software programs is required

TRAVEL REQUIREMENTS

Up to 10% of domestic or international travel is required

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act. 

Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center  ([email protected]) or contact AskGS to be directed to your accommodation resource.

Required Skills:



Preferred Skills:

Clinical Evaluations, Coaching, Critical Thinking, Drug Discovery Development, Entrepreneurship, Good Clinical Practice (GCP), Leadership, Medicines and Device Development and Regulation, Organizing, Regulatory Affairs Management, Relationship Building, Research Documents, Safety-Oriented, Scientific Research, Standard Scientific Processes and Procedures, Strategic Change, Study Management

The anticipated base pay range for this position is :

$117,000.00 - $201,250.00

For Bay Area:

$134,000.00 - $231,150.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company’s long-term incentive program.
Subject to the terms of their respective policies and date of hire, employees are eligible for the following time off benefits:
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 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 period10 days
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year
For additional general information on Company benefits, please go to: - https://www.careers.jnj.com/employee-benefits

Skills Required

  • Advanced degree in a scientific discipline
  • OD, MD/Ophthalmologist, or PhD in Vision Science or related field
  • Post-graduate training, residency, or fellowship
  • 5+ years of ophthalmic clinical research experience
  • Deep understanding of eye care, ophthalmic devices, or vision science
  • Experience supporting product development and lifecycle management
  • Led clinical studies or clinical programs (leadership experience)
  • Experience designing studies and selecting endpoints
  • Authored or substantially contributed to clinical study protocols
  • Authored or substantially contributed to Clinical Study Reports, abstracts, or manuscripts
  • Ability to interpret study results independently
  • Comfortable working with biostatisticians on sample size, endpoint strategy, SAPs, and result interpretation
  • Demonstrated ability to influence without direct authority and partner cross-functionally
  • Strong technical writing ability (protocols, reports, abstracts)
  • Understanding of biostatistics as applied to study data
  • Proficient with computers and software programs
  • Good Clinical Practice (GCP)
  • Regulatory affairs management experience

Johnson & Johnson Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Johnson & Johnson and has not been reviewed or approved by Johnson & Johnson.

  • Healthcare Strength Healthcare coverage is characterized as comprehensive across medical, dental, and vision, with added supports like onsite clinics, fitness centers, and Employee Assistance resources. Mental-health services and wellbeing reimbursements are also described as meaningful components of the overall package.
  • Retirement Support Retirement offerings are portrayed as a major differentiator, combining a 401(k) with employer matching and an employer-funded pension plan. Stock options and other long-term financial supports are also positioned as part of the broader rewards mix.
  • Parental & Family Support Family-related benefits are presented as notably strong, including paid parental leave for all new parents and additional leave types for caregiving and bereavement. Financial assistance for adoption, fertility treatment, and surrogacy is highlighted as a significant support.

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The Company
HQ: New Brunswick, NJ
143,612 Employees
Year Founded: 1886

What We Do

Profound Change Requires Boldness. Johnson & Johnson is the largest and most broadly based healthcare company in the world. We’re producing life-changing breakthroughs every day, and have been for the last 130 years. The combination of new technologies and your expertise enables amazing things to happen. Teams from J&J’s consumer business are creating digital tools to help people track the health of their skin. Those working in medical devices are 3-D printing artificial joints personalized for each patient, while researchers in pharmaceuticals use AI to discover lifesaving drugs. Imagine what the rest of our team of 134,000 people at 260 companies in more than 60 countries across the world is accomplishing. We redefine what it means to be a big company in today’s world. Social Media Community Guidelines: http://www.jnj.com/social-media-community-guidelines

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