Description

Job Title: Value and Access Principal AMCP Medical Writer

Onsite - Lake County Preferred

Purpose: Write and edit high-quality medically relevant AMCP dossiers for assigned therapeutics areas or assets to fulfill medical scientific and health economic objectives. Ensure successful preparation of high quality submission-ready documents and effective implementation of writing process and serve as AMCP dossier writing expert for the department.

Responsibilities:

- Responsible for but not limited to: developing editing and managing the production of AMCP Dossiers and scientific presentations for payers

- Collaborate with therapeutic area leads to incorporate TA strategies scientific platforms value messages into AMCP dossier

- Collaborate with Global Medical Information to develop and/or edit responses to address specific unsolicited payer and health care provider requests for health outcome information

- Analyze and interpret scientific data to update or develop comprehensive balanced credible and accurate documents that comply with applicable laws regulations guidances and policies and procedures and are used to appropriately respond to inquiries from payers and health care providers

- Provide medical writing support for multiple assets within a therapeutic areas

- Understand assimilate and interpret sources of information with appropriate guidance/direction from team members. Interpret and explain data generated from a variety of sources including internal and external studies research documentation charts graphs and tables and verify the results are consistent with study data. Perform literature searches for drafting AMCP dossiers

- Manages and prioritizes multiple projects provides solutions to complex problems and delivers complete and accurate information within deadlines

- Identify and propose solutions to resolve issues and questions arising during the writing/review process including resolution or elevation as appropriate

- Maintains awareness of current industry practices that pertain to Corporate Policies and Procedures. Must continually train/be compliant with all current industry and company requirements

- Complies with the reporting of adverse effects and product complaints to Pharmacovigilance and Surveillance

Skills

medical writing, regulatory

Top Skills Details

medical writing,regulatory

Additional Skills & Qualifications

Education:

PhD in Sciences or Technology, PharmD, or MD for Medical Writer III with 5+ years of experience in medical or scientific writing.

Nice to Haves:

Should have evidence of publications in peer-reviewed journals as first author and/or has written AMCP dossiers. Writers with prior experience in AMCP Format and AMCP Dossiers. Certification in oncology.

Job Type & Location

This is a Contract position based out of Mettawa, IL.

Pay and Benefits

The pay range for this position is $50.00 - $56.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully remote position.

Application Deadline

This position is anticipated to close on Feb 6, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.