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Clinical Research Manager - Jjmt Electrophysiology

2-8 years
$115,000 - $197,000 annually
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

Clinical Research Manager - JJMT Electrophysiology


Company

Johnson & Johnson MedTech (JJMT)


Location

Irvine, California, United States of America

Hybrid work schedule: onsite 2-3 days per week


Job Function

Discovery & Pre-Clinical/Clinical Development


Job Sub-Function

Clinical Development & Research – Non-MD


Job Category

Manager, Clinical Development & Research – Non-MD (PL7)


Requisition Number

R-029689


Date Posted

September 3, 2025


Application Deadline

October 3, 2025 (may be extended)


Company Overview

At Johnson & Johnson, we believe health is everything. Our expertise in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured with smarter, less invasive, and personalized solutions. Learn more: jnj.com


Role Overview

Johnson & Johnson MedTech, Electrophysiology is recruiting a Clinical Research Manager to join their Cardiovascular team in Irvine, CA. The team develops leading solutions for heart recovery, electrophysiology, and stroke, focusing on elevating standards of care for stroke, heart failure, and atrial fibrillation (AFib) patients.

As a Clinical Research Manager, you will provide leadership to Clinical Research Scientists within the Clinical Science & External Research (CSER) Team, ensuring timely, high-quality delivery of project goals and fostering strong internal relationships.


Key Responsibilities

  • Oversee study programs ensuring procedural compliance and risk management with appropriate escalation.

  • Prioritize research activities aligned with strategic objectives.

  • Track, validate, and communicate timelines, risks, and publication status.

  • Review program dashboards and summarize study details.

  • Manage execution of assigned pre-market and post-market collaborative studies, including protocol development and cross-functional approvals.

  • Ensure data collection and review compliance.

  • Represent the program in internal/external meetings.

  • Lead scientific aspects such as study design review, literature quality checks, and data accuracy.

  • Manage investigational product/device ordering, tracking, and accountability (as needed).

  • Interface with key opinion leaders and external researchers.

  • Collaborate with regional partners to standardize global processes.

  • Act as a trusted source of project knowledge for stakeholders.

  • Independently solve operational problems during clinical trial execution and escalate complex issues.

  • Communicate business issues and opportunities to management.

  • Ensure compliance with all company Health, Safety, Environmental, and regulatory guidelines.

  • Perform additional duties as assigned.


Qualifications

Required Education & Experience

  • Bachelor’s degree in Life Science, Physical Science, Nursing, Biological Science, or related field with at least 8 years clinical research experience OR

  • Master’s degree with at least 7 years clinical research experience OR

  • PhD with at least 5 years clinical research experience.

  • Previous experience managing or supervising global clinical trials.

  • Minimum 2 years leadership/management experience in clinical research, including people management.

  • Clinical project leadership across multiple studies/programs.

  • Strong cross-functional teamwork skills.

  • Experience with budget planning, tracking, and control.

  • Medical device industry experience.

  • Sound knowledge of ICH-GCP and clinical trial procedures.

Preferred Education & Experience

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

  • Clinical/medical background.


Other Information

  • Position may require up to 35% travel depending on program phase.

  • Primary location: Irvine, CA; remote work possible at management discretion.


Compensation & Benefits

  • Base salary range: $115,000 - $197,000 annually.

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

  • Benefits include medical, dental, vision, life insurance, disability, accident insurance, group legal insurance, pension, 401(k), and long-term incentives.

  • Paid time off includes:

    • Vacation (up to 120 hours/year)

    • Sick time (up to 40 hours/year; 56 hours/year for WA residents)

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

    • Work, personal, and family time (up to 40 hours/year)

More benefits info: jnj.com/employee-benefits


Equal Opportunity Employer Statement

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration regardless of race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status, or other legally protected characteristics. We actively seek qualified candidates who are protected veterans and individuals with disabilities.


Accommodation

Johnson & Johnson is committed to an inclusive interview process. Applicants with disabilities may request accommodations by contacting:

  • Employee Health Support Center: ra-employeehealthsup@its.jnj.com

  • Or AskGS for assistance.