Medical Writer
Spectraforce
Mettawa, Illinois
2 hours ago
Job Description
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:
Qualifications and Experience:
Education
Preferred Experience
Technical Skills
Additional Notes
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 50.00/hr.
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.
- 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.
Applicant Notices & Disclaimers
- For information on benefits, equal opportunity employment, and location-specific applicant notices, click here
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 50.00/hr.