Freelance AMCP Specialist - Rare Diseases

Key Responsibilities

• Develop and update AMCP dossiers for rare disease products, ensuring accuracy, clarity, and compliance with industry standards.
• Conduct literature reviews and synthesise clinical, economic, and real-world evidence into compelling narratives for healthcare decision-makers.
• Collaborate with internal stakeholders (HEOR, Medical Affairs, Market Access) to gather data and validate content.
• Ensure regulatory and labelling compliance across all dossier sections.
• Manage timelines and deliverables, providing regular progress updates to the client.
• Support payer engagement materials, including summary decks and evidence tables derived from the dossier.

Required Qualifications

• Proven experience developing AMCP dossiers within the rare disease field.
• Strong understanding of HEOR methodologies, real-world evidence, and payer requirements.
• Excellent writing and editing skills with attention to detail.
• Ability to work independently and manage multiple priorities in a remote setting.

Preferred Skills

• Familiarity with biotechnology and orphan drug market access challenges.
• Experience with digital collaboration tools (e.g., SharePoint, Teams).
• Knowledge of US healthcare system and formulary decision-making processes.

Engagement Details

• Contract Type: Freelance
• Schedule: Flexible within 25-35 hours/week
• Deliverables: Complete AMCP dossier and supporting payer materials within agreed timelines