Medical Affairs Scientist, Structural Heart (Irvine, CA) Johnson and Johnson MedTech, Electrophysiology

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 Affairs

Job Category:

Scientific/Technology

All Job Posting Locations:

Irvine, California, United States of America

Job Description:

Johnson & Johnson MedTech Electrophysiology is recruiting for a Medical Affairs Scientist, Structural Heart to join our team in Irvine, CA.

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/. 

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

About MedTech

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 Medical Affairs Scientist, Structural Heart.

Role Purpose

The Medical Affairs Scientist, Structural Heart will provide insights through literature and support the execution of company sponsored clinical trials and product evidentiary needs for safety and effectiveness assessments. This role will collaborate with R&D, Strategic Marketing, and Clinical Affairs to uncover insights on clinical and technology gaps and evidence that supports marketing messages through systematic reviews and meta-analyses, and strive to publish in peer-reviewed journals. In addition, the role will assist the study medical lead for clinical studies in adjudication of adverse events and concomitant medications. This position will require an individual with passion for scientific research.

What you will be doing:

In accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position:

• Perform scientific exploration including systematic reviews, meta-analyses, and literature analysis for research questions identified to understand clinical and technological gaps, device evidence, or disease state reviews.
• Write and publish peer-reviewed pieces including abstracts, posters, and articles. Possibility to present at conferences.
• Provide insights to collaborating functions including Research and Development (R&D), Global Strategic Marketing (GSM), Health Economics and Market Access (HEMA), and Clinical Affairs (CA).
• Support the recruitment and mentoring of interns that are typically 6-9 months long to increase scientific content exploration and publication.
• Provide support to study medical lead for company sponsored clinical studies, supporting the clinical trial team to execute on the study in a safe, effective, and timely manner.
• Contribute towards development and approval of clinical trial protocols, informed consents, investigator brochures, committee charters, and other study materials.
• Conduct routine review of adverse events (AEs), medical coding, source documents, and subject narratives.
• Contribute to drafting and review of study reports for assigned