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.
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