Medical Writer - Medical Information

3w3 weeks ago

Inizio Engage

US · Full-time · $95,000 – $130,000

About this role

Inizio Engage has a long-standing partnership with a leading Biotechnology company, across Commercial, Patient Solutions and Medical Affairs businesses. This is your opportunity to join Inizio Engage and represent a top biotechnology company as a Medical Writer focused on Medical Information.

In this hybrid role based in Titusville, NJ, you will create and review medical content for patients, HCPs, and payers, ensuring scientific rigor, balance, and impact. You will author standard and complex medical information responses, track recurring queries, and maintain a robust product response database.

You will serve as a subject matter expert for the therapeutic area, performing ongoing literature reviews and extracting complex data from scientific literature. You will also provide clinical guidance to assist in resolving escalated medical and access inquiries from the contact center.

This role offers the chance to work within an exceptional, collaborative culture recognized as a Best Place to Work in BioPharma and a Certified Great Place to Work. You will leverage your expertise to support quality and training initiatives for team members in partnership with leadership.

Requirements

Advanced Clinical/Science Degree (e.g. PhD, PharmD, or equivalent)
Excellent verbal, written and listening communication skills
3 or more years of relevant medical writing or medical information experience
Ability to create scientifically accurate, fair balanced, and impactful communications for patients, HCPs, and payers
Experience with literature review and data extraction from complex scientific literature
Knowledge of product review and approval processes (e.g., PRC, RDC)
Ability to serve as a subject matter expert and maintain in-depth product and therapeutic area knowledge

Responsibilities

Create and/or co-create and review medical content for patients, HCPs, and payers to ensure scientific rigor, balance, and impact
Author and review US MI responses by identifying and summarizing complex scientific literature in a scientifically accurate, fair balanced, and compliant manner
Track recurring queries and identify the need for creation of new standard responses
Perform ongoing literature reviews and extract complex data from scientific literature, arranging the data in an organized format
Provide clinical guidance and medical information to assist the resolution of escalated medical and/or access inquiries from the contact center
Serve as subject matter expert for the Therapeutic Area and maintain in-depth product and therapeutic area knowledge
Review derivative content and ensure alignment with MI responses and compliance with relevant review and approval processes
Leverage expertise to support quality and training initiatives for team members in partnership with leadership or client

Benefits

Competitive compensation
Excellent Benefits – accrued time off, medical, dental, vision, 401k, disability & life insurance, paid maternity and paternity leave benefits
Employee discounts and exclusive promotions
Recognition programs, contests, and company-wide awards
Exceptional, collaborative culture
Best Places to Work in BioPharma (2022, 2023, & 2025)
Certified Great Place to Work (2022, 2023, 2025, & 2026)