Associate Director, Global Publications

Associate Director, HEOR Publications

Location: Hybrid (New Jersey, USA)
Employment Type: Full-Time

About the Role

A leading, innovation-driven biopharmaceutical company is seeking an Associate Director, Global Publications to lead the development and execution of HEOR publication strategy across key therapeutic areas.

This individual will play a critical role in translating HEOR evidence into high-impact scientific communications and partner closely with cross-functional stakeholders across HEOR, medical affairs, clinical development, and market access to ensure a cohesive and strategically aligned evidence dissemination approach.

Key Responsibilities

HEOR Publications Strategy & Planning

• Lead the development and execution of HEOR publication plans, aligned with overall asset strategy and value evidence generation
• Identify opportunities to communicate economic, real-world, and outcomes data to support payer and access objectives
• Partner with internal stakeholders to ensure alignment across HEOR, medical affairs, and global publications strategy

Content Development & Execution

• Oversee development of HEOR-focused scientific deliverables, including:
  • Manuscripts, abstracts, and posters
  • Value dossiers and economic models summaries (as applicable)
  • Real-world evidence (RWE) and outcomes-based analyses

Cross-Functional Collaboration

• Collaborate closely with HEOR scientists, biostatistics, epidemiology, and clinical teams to ensure accurate interpretation and communication of data
• Partner with medical affairs and market access teams to align publications with broader evidence communication and stakeholder engagement strategies
• Engage with external experts, authors, and vendors to support high-quality publication development

Qualifications

• Advanced degree required: PhD, PharmD, MD, or MS
• ~7-10+ years of experience in HEOR & publications in the pharma/biotech industry
• Demonstrated experience developing and executing HEOR publication strategies
• Strong understanding of health economics methodologies (e.g., cost-effectiveness, budget impact, RWE analyses)
• Familiarity with global publication guidelines (ICMJE, GPP) and compliance frameworks
• Experience collaborating with cross-functional teams including market access, clinical, and medical affairs
• Excellent scientific writing, communication, and stakeholder management skills
• Ability to operate in a fast-paced, highly collaborative environment