Senior Clinical Research Scientist

Johnson Johnson; Irvine (CA); Presencial; USD 92 000 - 148 000; Tempo integral

Resumo da oferta

Johnson & Johnson is seeking a Senior Clinical Research Scientist in Irvine, CA, to support scientific publication and medical writing for the Electrophysiology business. This role focuses on drafting manuscripts, abstracts, posters, and web content while coordinating with global teams and external authors.

The ideal candidate has strong cardiovascular/ electrophysiology knowledge, excellent scientific writing skills, and familiarity with regulatory publication standards.

Qualificações

• Bachelor's Degree required; Advanced Degree preferred in Life Sciences, Physical Science, Nursing, Biological Science, or closely related field.
• 3+ years of direct involvement in clinical publications in a medical industry or related setting.
• 6+ years of scientific writing experience in a medical industry or related setting desired.
• 3+ years of cardiovascular and/or electrophysiology therapeutic areas experience preferred.

Responsabilidades

• Develop and deliver high-quality scientific manuscripts, abstracts, posters, and podium presentations for publication in peer-reviewed journals and major congresses.
• Draft dissemination materials (summaries, graphic abstracts, standard presentations, newsletters, webpages) for varied audiences.
• Collaborate with internal teams and external authors to ensure accuracy, alignment, and scientific integrity.
• Analyze and interpret clinical data; communicate data with well-structured tables and figures.
• Adhere to GCP, publication guidelines, and regulatory standards.
• Coordinate document review, feedback, approvals, and timely submissions.
• Monitor emerging trends in cardiovascular and electrophysiology to inform content development.
• Stay updated with current data by monthly literature reviews and sharing insights with global teams.
• Support clinical booth congress activities and gathering of evidence for cross-functional partners.

Conhecimentos

Communication skills

Project management

Interpersonal skills

Adaptability

GCP/GP/ICMJE knowledge

Scientific writing experience

Formação académica

Bachelor's degree in Life Sciences or related

Advanced degree preferred

Ferramentas

Publication management platforms

Reference software

Descrição da oferta de emprego

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

Job Description

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.

Purpose

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.

Responsibilities

• 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

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 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 & 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. I nternal employees contact AskGS to be directed to your accommodation resource.

#LI-Hybrid

Preferred Skills

• 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

Salary

$92,000.00 - $148,350.00

Benefits

ubject 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