New

Medical Writer

Spectraforce Technologies

Jan 29, 2026
Job Title: Medical Writer - Value and Access Principal AMCP Work Model: Onsite preferred; Lake County / Chicago area preferred - Remote candidates will be considered Assignment Length: 12 months to start (extension based on performance and budget) Role Overview: This role focuses on the development and management of high-quality AMCP dossiers to support payer and managed care decision-making. Due to an active backlog, the team is seeking an experienced medical writer who can jump in quickly with minimal ramp-up and take ownership of multiple dossiers simultaneously. The position is pan-therapeutic and requires strong hands-on medical writing skills along with the ability to lead cross-functional teams, manage timelines, and confidently communicate with senior scientific and medical stakeholders. This is a writing-first role, not a pure project management position. Key Responsibilities: Develop, write, edit, and manage submission-ready AMCP dossiers and payer-facing scientific materials. Lead AMCP dossier planning, kickoff meetings, timelines, and cross-functional collaboration. Work closely with Health Outcomes Research, Medical Payer Strategy, Therapeutic Area leads, and Global Medical Information teams. Incorporate therapeutic area strategies, scientific platforms, and value messages into dossiers. Conduct and synthesize literature reviews, clinical trial data, and health outcomes information. Analyze and interpret scientific and clinical data from internal and external sources, including Phase I-III trials. Translate complex scientific and statistical information into clear, balanced, and credible content for payer audiences. Support multiple assets and therapeutic areas simultaneously in a fast-paced environment. Manage review cycles, revisions, and approvals using document management systems such as Veeva. Identify and proactively resolve issues during the writing and review process. Ensure all content complies with applicable regulations, policies, and industry standards. Maintain compliance with adverse event reporting and product complaint procedures. Stay current with industry best practices related to medical writing and managed care communications. Qualifications and Experience: Education Advanced degree preferred: PhD, PharmD, MD, MS, DDS, or equivalent with relevant experience. Required Experience Strong experience in medical writing within pharma, biotech, or related environments. Pharma or industry experience. Demonstrated experience developing AMCP dossiers is highly preferred. Strong background in: Literature reviews Clinical trial data interpretation (Phase I-III) Scientific data synthesis and summarization Ability to manage multiple projects and lead cross-functional teams. Confidence in leading meetings, setting timelines, and managing stakeholders. Extensive publications experience (manuscripts, abstracts, posters), or Regulatory, payer-related, or outcomes-focused writing experience would be a bonus. Preferred Experience Experience in managed care, access, or formulary-related writing. HEOR or outcomes research exposure is a strong plus. Working knowledge of statistical concepts and interpretation (no analysis required). Technical Skills Highly proficient in Microsoft Word and PowerPoint. Experience with Excel, SharePoint, and Veeva preferred. Strong organizational, communication, and problem-solving skills. Additional Notes Onsite presence is preferred to support collaboration, but strong remote candidates will be considered. The role involves handling 2 to 3 AMCP dossiers at the same time. Candidates must be comfortable working independently, speaking up, and taking ownership. Senior candidates with extensive experience will be considered if aligned with the role. Accuracy and honesty around AMCP dossier experience is critical.