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Associate Director, Global Medical Affairs, Maternal-fetal Immunology
2 weeks ago
**Function**
- Medical Affairs Group
**Sub function**
- Medical Affairs
**Category**
- Director, Medical Affairs (PL9)
**Location**
- Horsham / United States of America
**Date posted**
- Jun 12 2025
**Requisition number**
- R-018528
**Work pattern**
- Hybrid Work
Description
**Job Function**:
Medical Affairs Group
** Job Sub Function**:
Medical Affairs
** Job Category**:
People Leader
** All Job Posting Locations**:
Horsham, Pennsylvania, United States of America
** Job Description**:
Johnson and Johnson is currently seeking an **Associate Director, Global Medical Affairs, Maternal-Fetal Immunology**located **in Horsham, PA.**
**About Immunology**
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 Immunology team leads in the development of transformational medicines for immunological disorders and illnesses. You can influence where medicine is going by restoring health to millions of people living with immune diseases.
Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.
The Associate Director, Global Medical Affairs, Maternal-Fetal Immunology (MFI)**,** will support the development and execution of medical affairs strategy for Nipocalimab for the ongoing Maternal-Fetal programs. The Associate Director will partner closely with several cross functional and cross regional stakeholders including the Regional Medical TA/product leaders, global commercial and market access leaders, Clinical Development Leaders, Compound Development Leaders, other R&D colleagues, GMA Operations Leader, etc., to develop integrated global medical affairs perspectives, strategies, and plans.
**Responsibilities include**:
- Contribute to the development and lead the execution of the Global Medical Affairs (GMAF) strategy and plan for MFI based on prioritized global and regional needs.
- MFI External Engagement: build and maintain relationships with key MFM specialists and adjunct HCP specialists, present MFI data and strategies to global KOLs through MAF core communication channels, and provide medical leadership with external stakeholders including professional and patient organizations, HA bodies, and the broader MFM community
- Collaborate closely with the regional medical affairs representatives to develop integrated global medical affairs strategies and plans and maintain open, two-way communication to ensure regional medical affairs is up to date on all plans, progress and decisions.
- Lead development and execution of the MFI global publication plan, review and approval of publications and scientific congress presentations, lead ongoing updates to MFI Scientific Communications Platform, and initiation and co-leadership of Publication Steering Committees to prepare for and execute Phase 3 trial data dissemination
- Develop Global Integrated Evidence Generation Plan (IEGP), including RWE strategy and objectives, ensuring alignment with overall GMAF and Brand strategy for MFI, coordinating with regional and cross-functional stakeholders to build and periodically update evidence catalogues.
- Lead Global medical training on MFI indications, including development of novel training resources, ensuring pull-through of key concepts and messages by regional and cross-functional stakeholders
- Co-lead the asset specific cross regional medical affairs strategic discussions (MAST) and cross-regional knowledge transfer and scientific exchange meetings ( WISE) for MFI.
**Requirements**:
- An advanced scientific/medical degree (e.g. MD, PhD, or PharmD) is required.
- Experience in Maternal-Fetal Immunology or Autoantibody is highly preferred
- A minimum of 3 years of combined relevant experience in a medical/clinical environment and/or scientific function in the pharmaceutical industry is required.
- At least three years in the Medical Affairs environment is highly preferred.
- A demonstrated track record of success within Medical Affairs, clinical environment and/or scientific function is required.
- Highly innovative with the ability to drive a complex and changing environment and effectively manage and resolve issues is required
- Global mindset and ability to partner cross culturally/regionally is required
- In-depth knowledge of study/clinical methodology, study/clinical data reviews and analysis is preferred
- A demonstrated track record leading highly matrixed, cross-functional work teams comprised of high-level managers and executives is required.
- Experience developing and managing strategic relationships with medical experts/opinion leaders is required
- Proven ability to act as a Scientific Matter Expert for external audiences is required.
- Excellent knowledge of study execution, benefit risk management and life-cycle management are preferred
- Proven
