Medical Writer

Role Overview

• Create and/or co-create and review medical content for patients, HCPs and payers to ensure scientific rigor, balance and impact, this includes field medical slides (Medical Science Liaisons and Managed Care Liaisons), and standard or complex medical information responses.
• Track recurring queries and identify need for creation of new standard responses
• As needed, provide medical review for scientific accuracy and provide input on the development/use of scientific and promotional materials consistent with approved client processes and policies (Product Review Committee [PRC], Reprint Dissemination Committee[RDC]) and in close partnership with client Medical Content Strategy Leads and MI leadership team to identify and address training needs of Medical Information and Communications staff, internal partners, or external vendors.
• Write, review, edit and deliver medical content for training purposes, as needed.
• Author and review US MI responses by identifying and summarizing complex scientific literature in a scientifically accurate, fair balanced, concise and compliant manner to help inform clinical decision-making by HCPs.
• Plan and maintain a robust product response MI database including launch readiness plans that meets the scientific needs of customers
• Serve as subject matter expert for the Therapeutic Area and maintains in-depth product and therapeutic area knowledge
• Perform ongoing literature reviews and extracts complex data from scientific literature and arranges 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
• Utilize internal scientific narratives and employing creative data visualization techniques to the develop medical resources and tools, enhancing scientific engagement through compelling content practices
• Review of complex and/or escalated MI cases
• Review derivative content and ensuring alignment with MI responses and compliant with relevant review and approval process
• Provide relevant stakeholders with actionable insights and recommendations based on knowledge of product/therapeutic area
• Create and/or update reference materials and data on file summaries
• Leverage expertise to support the quality and training initiatives for team members in partnership with leadership and or client, as appropriate

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 communication experience with Neurology experience highly preferred
• 3 or more years of direct medical information and/or relevant medical affairs experience in the pharmaceutical industry, a clinical setting or equivalent background and experience
• Proficient in Google Workspace and Office 365
• Ability to work both independently and within a group setting
• Ability to proficiently operate computer hardware and software on a daily basis

Benefits

• Competitive compensation
• Excellent Benefits – accrued time off, medical, dental, vision, 401k, disability & life insurance, paid maternity and paternity leave benefits, employee discounts/promotions
• Employee discounts & 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)