Medical Director, Global Medical 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 Affairs – MD

Job Category:
Scientific/Technology

All Job Posting Locations:
Raritan, New Jersey, United States of America

Job Description:

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements.

Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Our Oncology team is focused on the elimination of cancer by discovering new pathways and modalities to finding treatments and cures.

We lead where medicine is going and need innovators with an unwavering commitment to results.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

The Medical Director, Global Medical Affairs, known also as the Study Responsible Physician (SRP) is accountable for the medical and scientific oversight of assigned clinical studies within the Global Medical Affairs function.

This role ensures the integrity of study design, execution, and reporting, and serves as the primary medical contact for internal and external stakeholders.

Key Responsibilities



* Provide medical leadership and oversight for assigned Medical Affairs studies.


* Collaborate with cross-functional teams to ensure scientific integrity and operational excellence.


* Review and approve study protocols, informed consent forms, medical review plans and other study-related documents.


* Serve as the primary medical contact for investigators and study teams.


* Support regulatory and compliance activities related to study execution.


* Contribute to data analysis, interpretation, and dissemination of study results.


* Ensure alignment with the Integrated Evidence Generation Plan (IEGP).

Qualifications



* MD or equivalent medical degree required.


* Board certification in Oncology highly preferred.


* Minimum of 5 years of experience in clinical research or medical affairs.  Experience as SRP in R&D highly preferred.


* Experience in study design and execution within pharmaceutical or biotech industry.

The expected base pay range for this position is $182K - $315K.

The Company maintains highly competitive, performance-based compensation programs.  Under current guidelines, this position is eligible for an annual per...