Medical Writer
Job in
Titusville, Mercer County, New Jersey, 08560, USA
Listed on 2026-03-01
Listing for:
Motion Recruitment
Full Time
position Listed on 2026-03-01
Job specializations:
-
Healthcare
Healthcare Administration, Health Communications, Healthcare Management
Job Description & How to Apply Below
Contractor Medical Writer – Medical Information, Payer & Health Systems
Location: Titusville, NJ
Contract Duration: March 16, 2026 – December 31, 2027
Compensation: Pay based on experience
About the RoleWe are seeking a Medical Writer to support the creation and delivery of scientific materials for Payers, Healthcare Intermediaries, and Health Systems. This role focuses on translating clinical data into clear, evidence-based content that helps external healthcare decision-makers understand the value of our products.
You will work closely with Medical Affairs, Real-World Value & Evidence (RW V&E), and cross-functional partners to ensure materials are accurate, compliant, and delivered on time.
Key Responsibilities Scientific Content Development (70%)- Develop and update evidence-based materials for payer audiences.
- Support creation of AMCP dossiers (standard and pre-approval), Medicaid formulary submissions, and customized payer responses.
- Participate in cross-functional review and approval of regulated payer content.
- Collaborate with Medical Affairs and RW V&E teams to align scientific messaging with clinical and value data.
- Support development of digital payer materials.
- Assist with responses to unsolicited medical information requests from payers and health systems.
- Support compendia interactions and vendor material review for scientific accuracy and quality.
- Analyze payer feedback and engagement data.
- Help track performance metrics and identify opportunities to improve content effectiveness.
- Support special projects as assigned.
- Conduct landscape research related to payers, healthcare intermediaries, and health systems.
- Bachelor’s degree in a scientific, medical, or healthcare-related field.
- 3+ years of experience in Medical Information, Medical Affairs, payer communications, or pharmaceutical medical writing.
- Experience developing scientific materials in a regulated pharmaceutical environment.
- Strong scientific writing and data interpretation skills.
- Ability to work cross-functionally in a matrixed organization.
- Excellent attention to detail and project management skills.
- Advanced degree (Pharm
D, PhD, MD, or other relevant clinical/scientific degree). - Experience developing AMCP dossiers, pre-approval dossiers, or formulary submissions.
- Familiarity with payer audiences and health system stakeholders.
- Experience working with Real-World Evidence (RWE) and health economics data.
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