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Clinical Research Scientist - JJMT Electrophysiology

Johnson & Johnson
United Statesfull_timeVerifiedPosted 6 Aug 2025
💰 $143,000/yr($89,000/yr$143,000/yr)

About the role

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 https://www.jnj.com

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 Clinical Research Scientist to JJMT Electrophysiology. This role is based in Irvine, CA and reports to the office on assigned days 2-3 times per week.

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 https://www.jnj.com/.

Summary:

This professional will report to Clinical Science and External Research (CSER) Leaders in the management of assigned clinical projects for the Cardiovascular Group to support the development of the evidence generation and dissemination strategy of assigned products, manage external clinical studies, execute publication plans, and conduct literature reviews. S/he will manage activities with supervision consistent with level of experience. S/he will be responsible for providing support activities for clinical activities and other study-related tasks, as well as applicable department study-related procedures.

Job Responsibilities:

The Clinical Research Scientist will or may be responsible for:

  • Working with Global Strategic Marketing, Franchise Clinical Leaders, Biostatistics, Data Management, Medical Affairs, and other functions on: (i) Executing research collaborations with physicians, (ii) tracking study idea development and progress, and (iii) planning data dissemination via congress presentation and peer-reviewed publications
  • Managing nonregulated studies (e.g., Investigator initiated, Registries, Real-world evidence, Company -sponsored post market studies) and low complexity regulated studies (eg., Post approval, Real-world evidence) including study budget assessment, fair market value appraisal, contract development and execution, and payments
  • Interfacing and collaborating with investigators, IRBs/ECs, Competent Authorities, contractors/vendors, and Company personnel
  • Developing study-related materials (e.g., protocol, CRFs, CSR)
  • Analyzing, interpreting, summarizing, and sharing appropriate interpretation of clinical evidence generated from research studies
  • Executing study-related publication efforts including abstracts, congress presentations, and manuscripts, per clinical publication policy
  • Collaborating with cross-functional team members to develop collaterals to disseminate research results among internal and external stakeholders
  • Knowing, understanding, incorporating, and complying with all applicable laws and regulations relating to business activities, and Policies and Procedures
  • Evaluating publication support requests and providing meaningful, consolidated comments during the publication development lifecycle
  • Tracking assigned project budgets to ensure adherence to business plans
  • Communicating progress towards planned timelines

Qualifications:

  • A minimum of a Bachelor’s degree with at least 2 years of clinical research experience required
  • Advance degree (Master’s degree, PhD, PharmD etc.) with 0-1 year of clinical or related research experience highly preferred
  • A Life Science, Physical Science, Nursing, or Biological Science degree is preferred
  • Ability to analyze and interpret scientific data and advanced writing/presentation skills are required, such as conducting literature reviews, and planning and drafting conference presen

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Company

Johnson & Johnson

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