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Senior Clinical Research Specialist - Jjmt Electrophysiology

4 years
$89,000 to $143,750
10 Sept. 10, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/ B.Pharma/ M.Pharma/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Senior Clinical Research Specialist - JJMT Electrophysiology


Company

Johnson & Johnson


Locations

  • Irvine, California (Primary)

  • Remote candidates accepted within the United States (multiple states and cities listed as examples, open nationwide)

Examples of states include:
Alabama, Arizona, Arkansas, Colorado, Connecticut, Delaware, Florida, Georgia, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming


Work Pattern

Hybrid Work


Job Category

Experienced Scientist, Clinical Development & Research – Non-MD (ST5)


Job Function

Discovery & Pre-Clinical/Clinical Development


Job Sub Function

Clinical Development & Research – Non-MD


Job Posting Details

  • Date Posted: September 8, 2025

  • Requisition Number: R-030337

  • Application Deadline: October 10, 2025 (may be extended)

  • Apply at: www.careers.jnj.com


Company Overview

Johnson & Johnson is a global healthcare innovator focusing on preventing, treating, and curing complex diseases. They emphasize developing smarter, less invasive, and personalized treatments through expertise in Innovative Medicine and MedTech. The MedTech Electrophysiology team focuses on cardiovascular solutions including heart recovery, electrophysiology, and stroke.

Learn more:


Role Summary

The Senior Clinical Research Specialist supports clinical trials in the Clinical R&D Department for Biosense Webster within the MedTech Electrophysiology division. This role involves managing clinical trial execution, compliance, and collaboration across multiple stakeholders to drive successful study outcomes.


Key Responsibilities

  • Support execution of company-sponsored clinical trials ensuring compliance with timelines and milestones.

  • Oversee feasibility, selection, setup, conduct, and closure of clinical trials within allocated countries, complying with ICH-GCP, legislation, and SOPs.

  • Serve as a primary contact for clinical trial sites and manage site relationships.

  • Contribute to development of clinical trial documents: study protocols, informed consent forms, case report forms (CRFs), monitoring plans, study manuals, investigator brochures, and annual reports.

  • Ensure trial registration on clinicaltrials.gov and support publications.

  • Manage investigational products and trial materials including ordering, tracking, and accountability.

  • Collaborate with site personnel, Institutional Review Boards/Ethics Committees (IRBs/ECs), contractors/vendors, and internal teams.

  • Supervise development and execution of Investigator agreements and trial payments.

  • Review clinical data to prepare for statistical analyses and publications.

  • Perform monitoring activities (site qualification, initiation, interim, close-out visits) as needed.

  • Support global evidence generation and dissemination strategies.

  • Provide procedural compliance and data collection support on-site if applicable.

  • Critically assess literature and contribute to evidence interpretation and dissemination.

  • Deliver assigned clinical projects on time, within budget, and compliant with regulations and SOPs.

  • Communicate business issues/opportunities to management; serve as a reliable project knowledge resource.

  • Support project/study budget activities.

  • Develop strong understanding of product pipeline and business needs.

  • Ensure personal and company compliance with all relevant regulations and policies.

  • Perform other duties as assigned.

  • Work generally supervised, with independent decision-making on simple and some complex issues under mentorship.


Qualifications

Education

  • Minimum Bachelor’s Degree required, preferably in Life Science, Physical Science, Nursing, or Biological Science.

Experience

  • BS degree with minimum 4 years relevant experience, MS with 3 years, or PhD with 2 years.

  • Previous clinical research experience in medical devices, particularly interventional cardiology or electrophysiology, strongly preferred.

  • Relevant certifications preferred (e.g., CCRA, CCRC, CCRP, RAC, CDE, GCP, ISO 14155, MDR, MEDDEV).

  • Clinical or medical background is a plus.

Skills and Competencies

  • Good understanding of clinical research science, processes, trends, and global trial regulations.

  • Proven ability to support delivery of clinical projects on time, within budget, and compliant with SOPs/regulations.

  • Strong presentation and technical writing skills.

  • Excellent written and oral communication skills.


Compensation

  • Base Pay Range: $89,000 to $143,750 (anticipated)

  • Eligible for annual performance bonus based on individual and company performance.

  • Eligible for long-term incentive program.


Benefits

  • Medical, dental, vision, life insurance

  • Short- and long-term disability

  • Business accident insurance, group legal insurance

  • Retirement plans: pension and 401(k) savings plan

  • Paid time off:

    • Vacation: up to 120 hours/year

    • Sick time: up to 40 hours/year

    • Holidays (including floating holidays): up to 13 days/year

    • Work, Personal and Family Time: up to 40 hours/year

More info: Employee Benefits


Equal Opportunity Employer Statement

Johnson & Johnson is committed to equal employment opportunity regardless of race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status, or other protected characteristics. The company actively seeks qualified protected veterans and individuals with disabilities.


Accommodation Statement

Applicants with disabilities needing accommodation during the interview process can contact:

  • Email: ra-employeehealthsup@its.jnj.com

  • Or contact AskGS for accommodation resources.