- Location: New Jersey, United States
- Type: Contract
- Job ID: 10308
- Work Setting: On-Site
- Posted: May 4, 2026
- Closing Date: May 17, 2027
- Tax Status: W2
Medical-Payer Evidence Translation Consultant
12 month contract
Remote, EST hours
Job Summary
The Medical-Payer Evidence Translation Consultant will support the development, approval, training, and deployment of scientific and value-evidence materials used in engagements with payers and healthcare decision-makers (HCDMs). This role will lead the operational execution of payer-facing resources, including Disease State Education (DSE), Pre-Approval Information Exchange (PIE), and Healthcare Economic Information (HCEI) materials, while partnering across Medical Affairs, Value Evidence, Medical Strategy, Market Access, field teams, and external vendors.
Job Responsibilities
- Translate clinical, economic, outcomes, and real-world evidence into clear, compliant, payer-focused scientific materials.
- Lead development and execution of DSE, PIE, HCEI, and other payer/HCDM-facing resources.
- Manage content development from storyboard and drafting through review, approval, training, and field deployment.
- Lead project timelines, milestones, deliverables, meetings, and cross-functional stakeholder coordination.
- Manage external agencies/vendors, including SOWs, purchase orders, budgets, and project communications.
- Coordinate promotional and non-promotional medical review and approval processes.
- Support training and field readiness for approved payer-facing resources.
- Collect and synthesize payer insights to identify evidence needs, content gaps, and opportunities for future enhancements.
Qualifications
- Advanced degree (PhD, PharmD, MD, or MPH) in a relevant scientific or health-related field.
- 7+ years of pharmaceutical industry or equivalent relevant experience.
- Strong understanding of managed care, payer communications, HCEI, RWE, and applicable FDA guidance.
- Experience developing scientific, medical, and/or value-evidence resources for payer or HCDM engagement.
- Strong medical communications and scientific evidence-translation experience.
- Demonstrated cross-functional project leadership and ability to manage multiple projects simultaneously.
- Experience managing external agencies/vendors.
- Strong communication, stakeholder management, organizational, and operational execution skills.
- Veeva promotional/medical review experience and contracting/budget management experience strongly preferred.
- CNS, Nephrology, Immunology, and/or rare disease experience preferred.