Freelance AMCP Specialist - Rare Diseases
EPM Scientific are partnering with a longstanding global Biotechnology Research/Consultancy client who is urgently seeking a Freelance AMCP Dossier Specialist to support the development of high-quality, evidence-based dossiers for rare disease therapies. This role will involve close collaboration with cross-functional teams to ensure compliance with AMCP Format and alignment with payer and formulary requirements.
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
If interested, please click the relevant links to apply!
We look forward to hearing from you.
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