Johnson & Johnson

Staff Clinical Research Scientist

Johnson & Johnson$109K — $174K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in Life Sciences or related field
  • 5+ years of experience in scientific publications
  • Exceptional written and oral communication skills
  • Strong project management capabilities
  • Excellent interpersonal skills for cross-functional collaboration
  • Adaptability to fast-paced environments
  • Knowledge of Good Clinical Practice and publication standards

Responsibilities

  • Develop and deliver scientific manuscripts, abstracts, and presentations
  • Collaborate with internal and external teams for content accuracy
  • Support strategic publication plans for key clinical studies
  • Analyze and communicate clinical data effectively
  • Adhere to guidelines for ethical publication development
  • Coordinate document reviews and submissions
  • Stay informed on emerging trends in electrophysiology

Benefits

  • Vacation - 120 hours per year
  • Sick time - 40 hours per year (varies by state)
  • Holiday pay - 13 days per year
  • Up to 40 hours of personal and family time per year
  • Parental leave - 480 hours within the first year after birth/adoption
  • Bereavement leave - 240 hours for immediate family
  • Volunteer leave - 32 hours per year
Full Job Description
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 Staff 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.

The Staff 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 writing and managing manuscripts, abstracts, posters, and presentations that support peer-reviewed publications and congress activities. 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.

Key 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
  • 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
  • Support the strategic publication plan for key products and studies, including first-in-human trials, pivotal studies, indication expansions, postmarket surveillances, and registries
  • 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 publications while continuing to look at innovation in publication and scientific communications
  • 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
  • Track publication metrics, congress submissions, and support database management using publication tools and systems
  • Stays on top of current scientific data by participating in monthly literature review and sharing key insights with global teams
  • Support congress planning, including participating in clinical booth activities and gathering of scientific evidence to be shared with company
  • Engage with Clinical Science & External Research associates and cross-functional teams to develop evidence dissemination materials tailored to various internal and external audiences (ie, field personnel, HCPs, investors)


Qualifications

Required:
  • Minimum of a Bachelor's Degree in Life Sciences, Physical Science, Nursing, Biological Science, or closely related field
  • Minimum of 5+ years of direct involvement in scientific publications in a medical industry or related setting
  • 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


Preferred:
  • PhD/MD/PharmD with industry/academic research experience
  • 8+ years of scientific writing experience in a medical industry or related setting
  • 3+ years of experience in cardiovascular and/or electrophysiology therapeutic areas
  • Familiarity with publication management platforms and reference software
  • ISMPP CMPP™ or AMWA MWC® credentials
  • Knowledge of electrophysiology procedures and terminology


Other:
  • May require up to 10% travel


#LI-Hybrid

Required Skills:

Preferred Skills:

The anticipated base pay range for this position is :
$109,000.00 - $174,800.00

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

About Johnson & Johnson

Scio Diamond creates single-crystal Type IIa diamonds for the jewelry market and for industrial applications. It employs a patent-protected chemical vapor deposition (CVD) process in a precisely controlled laboratory setting to produce diamonds. It was founded in 2009 and is headquartered in Greenville, South Carolina.

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Learn more about Johnson & Johnson
Size
141,700 employees
Market Cap
$462.7 billion
Industry
Net Income
$14.7 billion
Founded
1886
5 Year Trend
+5.5%
Revenue
$82.5 billion
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