New · posted Nov 11
Johnson & Johnson · Medical Devices
Senior Clinical Research Scientist EP
- Irvine, CA
- Hybrid
- Full-time
- Senior & Principal
The role
The Senior Clinical Research Scientist will join the Clinical Science & External Research (CSER) Team responsible for global evidence dissemination of scientific findings from clinical trials and registries sponsored by Johnson & Johnson MedTech Electrophysiology. This associate will play a critical role in the creation and delivery of accurate, high-quality scientific content that communicates clinical and real-world data on the Company’s Electrophysiology medical devices. This role is responsible for drafting manuscripts, abstracts, posters, and presentations that support peer-reviewed publications and congress activities. This associate will also support the creation of summaries, graphic abstracts, webpages, and other deliverables to support the broad dissemination of clinical data from Company studies. The ideal candidate will have strong scientific writing experience, deep familiarity with the cardiovascular and/or electrophysiology clinical landscapes, and a thorough understanding of publication standards, regulatory guidelines, and clinical study design.
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.
Johnson and Johnson is currently seeking a Senior Clinical Research Scientist to support the scientific publication medical writing needs of the Electrophysiology business. This role is based in Irvine, CA and reports to the office on assigned days 2-3 times per week.
What you need
Qualifications/Requirements
- Minimum of a Bachelor's Degree required; Advanced Degree preferred. Life Sciences, Physical Science, Nursing, Biological Science, or closely related field required.
- Minimum of 3+ years of direct involvement in clinical publications in a medical industry or related setting required. Industry/academic research experience strongly preferred.
- 3+ years of experience in cardiovascular and/or electrophysiology therapeutic areas preferred.
- Familiarity with publication management platforms and reference software preferred.
- ISMPP CMPP™ or AMWA MWC® credentials preferred.
- Knowledge of electrophysiology procedures and terminology strongly preferred.
- Excellent written and oral communication skills
- Strong project management skills to balance multiple projects
- Excellent interpersonal skills, with the ability to build relationships and collaborate effectively with key partners across different time zones
- Demonstrated adaptability in fast-paced, evolving environments
- Knowledge of Good Clinical Practice, Good Publication Practice, and ICMJE Standards
- 6+ years of scientific writing experience in a medical industry or related setting desired.
Johnson & 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, external applicants please contact us via https://www.jnj.com/contact-us/careers. Internal employees contact AskGS to be directed to your accommodation resource.
Preferred Skillsnice to have
AI Judgement Integration, Analytical Reasoning, Clinical Data Management, Clinical Evaluations, Clinical Trial Protocols, Coaching, Consulting, Data Savvy, Drug Discovery Development, Good Clinical Practice (GCP), Medicines and Device Development and Regulation, Persistence and Tenacity, Regulatory Affairs Management, Research Documents, Resource Management, Safety-Oriented, Scientific Research, Technologically Savvy
What you'll do
- Develop and deliver high-quality scientific manuscripts, abstracts, posters, and podium presentations for publication in peer-reviewed journals and presentation at major cardiovascular and electrophysiology congresses
- Draft evidence dissemination materials (eg, summaries, graphic abstracts, standard presentations, newsletters, webpages) tailored to various internal and external audiences (ie, field personnel, HCPs, investors)
- Collaborate closely with internal cross-functional teams (Clinical, Biostatistics, Medical Affairs, Global Strategic Marketing, Health Economics and Market Access) and external physician authors to ensure accuracy, alignment, and scientific integrity
- Analyze and interpret clinical data; effectively communicate data using well-structured tables and visually compelling figures
- Adhere to external guidelines and Company policies governing the ethical development of clinical data
- Coordinate document review, incorporate feedback, obtain approvals, and ensure timely submissions
- Maintain awareness of emerging trends and competitors in cardiovascular and electrophysiology therapy spaces to inform content development
- Stays on top of current scientific data by participating in monthly literature review and sharing key insights with global teams
- Support clinical booth congress activities and the gathering of scientific evidence to be shared with cross-functional partners
Pay and benefits
$94,000 – $151,800 a year
Employer providedThe anticipated base pay range for this position is
$94,000.00 - $151,800.00
Vacation 120 hours per year
Sick time 40 hours per year
13 paid holidays
Parental leave 480 hours
Bereavement leave
Volunteer leave 32 hours per year
Where you'll work
Irvine, CAHybridOpen in Maps (opens in a new tab)
More jobs in Irvine, CAWorking conditions
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
Equal opportunity, accessibility and legal noticesJohnson & Johnson's statements, word for word
Additional Description for Pay Transparency
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
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.
Job intelligence
The context around this role
Live data · November 11, 2026
Salary intelligence
How the pay compares
This role's midpoint is 12% below the US median for Clinical Evaluation & Medical Writing roles at this level.
This roleEmployer provided
Senior & Principal roles in California6 roles publishing pay
Senior & Principal roles in the US13 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $94,000 | — | $151,800 |
| California (middle half) | $126,000 | $137,500 | $190,625 |
| All US (middle half) | $123,000 | $140,000 | $171,000 |
This role: Johnson & Johnson's own published range. Comparisons: the base pay employers published on open Clinical Evaluation & Medical Writing roles at the same level on Regulatory Jobs, November 11, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Evaluation & Medical Writing
The general path across 40 open Clinical Evaluation & Medical Writing roles on Regulatory Jobs, with the titles they carry most. Not Johnson & Johnson's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 27 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership8
- Documentation and SOPs6
- Clinical trial conduct3
- GMP and compliance2
- Data and digital systems2
- Lab testing and methods1
- Regulatory submissions1
Regulatory intelligence
The rules, regulations and standards behind this role
The regulations, guidance and standards that govern Clinical Evaluation & Medical Writing work in medical devices, led by the one this posting names, each linked to the agency or standards body that publishes it.
- ICHICH E6(R3) good clinical practice(official source, opens in a new tab)The international standard for the design, conduct and reporting of clinical trialsNamed in the posting
- EUMDCG guidance(official source, opens in a new tab)The Medical Device Coordination Group's endorsed guidance on applying the MDR and IVDR
- EUEU MDR (Regulation 2017/745)(official source, opens in a new tab)The EU Medical Device Regulation: CE marking, technical documentation, vigilance
- ISOISO 14155(official source, opens in a new tab)Good clinical practice for clinical investigations of medical devices
- ISOISO 14971(official source, opens in a new tab)Application of risk management to medical devices
- ICHICH E9 and E9(R1)(official source, opens in a new tab)Statistical principles for clinical trials and estimands
- FDA21 CFR Part 812(official source, opens in a new tab)Investigational device exemptions for clinical studies of devices
- FDAFDA 510(k)(official source, opens in a new tab)Premarket notification: showing substantial equivalence to a legally marketed device
- FDA21 CFR Part 814(official source, opens in a new tab)Premarket approval of class III medical devices
- FDAFDA De Novo(official source, opens in a new tab)Classification requests for novel low- to moderate-risk devices
- EUEU IVDR (Regulation 2017/746)(official source, opens in a new tab)The EU In Vitro Diagnostic Medical Devices Regulation
- NIH42 CFR Part 11(official source, opens in a new tab)Clinical trial registration and results reporting on ClinicalTrials.gov
- IECIEC 62366-1(official source, opens in a new tab)Application of usability engineering to medical devices
- FDAFDA human factors guidance(official source, opens in a new tab)Applying human factors and usability engineering to medical devices
- FDA21 CFR Part 803(official source, opens in a new tab)Medical device reporting of deaths, serious injuries and malfunctions
- IMDRFIMDRF(official source, opens in a new tab)International Medical Device Regulators Forum guidance, including software as a medical device
From Regulatory News
Company hiring pulse
Johnson & Johnson on Regulatory Jobs
- 42
- Open roles
- 42
- Distinct roles
- 18
- Locations
By discipline
- Quality25 60%
- Clinical9 21%
- Regulatory8 19%
By level
- Manager16 38%
- Senior & Principal15 36%
- Associate & Specialist7 17%
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Senior Clinical Research Scientist EP at Johnson & Johnson
Applications close November 17. $94K–$152K a year, employer provided.