Johnson & Johnson MedTech is hiring : Senior Analyst, Medical Writing, Clinical &

Senior Analyst, Medical Writing, Clinical & Regulatory Affairs

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 : Medical Affairs Group

Job Sub Function : Medical Writing

Job Category : Professional

Job Locations : Danvers, Massachusetts, United States of America, Remote (US)

About Cardiovascular

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments. Are you passionate about improving and expanding the possibilities of Cardiovascular? Ready to join a team that’s reimagining how we heal? Our Cardiovascular team develops leading solutions for heart recovery, electrophysiology, and stroke. You will join a proud heritage of continually elevating standards of care for stroke, heart failure and atrial fibrillation (AFib) patients. Your unique talents will help patients on their journey to wellness. Learn more at https : / / www.jnj.com / medtech

We are searching for the best talent for a Senior Analyst, Medical Writing, Clinical & Regulatory Affairs. This is a remote role available in the continental USA.

Purpose

The Senior Analyst, Medical Writing, Clinical & Regulatory Affairs will contribute to clinical evaluation activities within the Clinical and Regulatory Affairs department. The ideal candidate will be versed in clinical evaluation and be able to directly influence current and new submissions and updates.

You Will Be Responsible For

• Plan, prepare, and finalize regulatory documents focused on global post‑market surveillance requirements, particularly US and EU; these include, but are not limited to, clinical evaluation plans and reports, post‑market surveillance plans, summary of safety and clinical performance (SSCP), and post‑market clinical follow‑up plans and reports (PMCF)
• Conduct literature reviews and clinical data reviews to support preparation of regulatory documents and submissions
• Support cross‑functional document planning and review through collaboration with colleagues across departments
• Ensure all regulatory documents meet regulatory requirements and guidelines (e.g., FDA, EMA) and company standards
• Stay updated with regulatory guidelines, industry trends, and best practices in regulatory medical writing
• Opportunities to expand writing capabilities in other areas of Clinical & Regulatory Affairs

Qualifications / Requirements

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants’ needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https : / / www.jnj.com / contact-us / careers internal employees contact AskGS to be directed to your accommodation resource.

The anticipated base pay range for this position is : $91,000-$147,200

Additional Description For Pay Transparency

Subject to the terms of their respective plans, employees and / or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs : medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance. Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Company’s long-term incentive program. 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 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 Condolence Leave – 30 days for an immediate family member : 5 days for an extended family member Caregiver Leave – 10 days Volunteer Leave – 4 days Military Spouse Time-Off – 80 hours Additional information can be found through the link below. https : / / www.careers.jnj.com / employee-benefits

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