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Senior Medical Writer

Remote / Online - Candidates ideally in
Charlotte, Mecklenburg County, North Carolina, 28245, USA
Listing for: Regeneron
Remote/Work from Home position
Listed on 2026-07-29
Job specializations:
  • Research/Development
    Clinical Research
Salary/Wage Range or Industry Benchmark: 128600 - 210000 USD Yearly USD 128600.00 210000.00 YEAR
Job Description & How to Apply Below

Senior Medical Writer – Global Development

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking a Senior Medical Writer to join our Medical Writing team, supporting clinical document delivery across Global Development in a remote work mode. In this role, you will author clinical study reports, protocols, consent forms, narratives, and investigator brochures while collaborating with clinical teams and biostatisticians.

When

& Where

United States or United Kingdom (remote)

Discover Your Role
  • Author clinical study reports (CSRs), protocols, informed consent forms (ICFs), narratives, investigator brochures, and other regulatory documents across therapeutic areas.
  • Represent Medical Writing at meetings, drive document development, and articulate strategy and timelines.
  • Identify the right parties for content decisions and synthesize discussions into clear, accurate prose.
  • Review work of junior or outsourced writers and CSR‑related documents such as Statistical Analysis Plans and TFLs.
  • Write plain‑language content such as ICFs and explain complex medical concepts to lay audiences.
  • Adhere to applicable guidelines, templates, SOPs and internal training while contributing to process improvement across Medical Writing and Global Development.
  • Mentor junior staff, manage multiple priorities and foster collaboration to resolve conflict.
This Role Requires
  • Bachelor's degree required; advanced degree preferred.
  • Minimum 3 years of medical writing experience, including working knowledge of biostatistics.
  • Strong knowledge of the clinical research process and applicable regulations, including ICH GCP.
  • Clinical document reading, writing, and editing experience.
  • Strong knowledge of MS Word, Adobe Acrobat, PowerPoint, and electronic document management systems.
  • Ability to manage multiple projects with strong organisational, interpersonal, and communication skills.
Salary Range (annually)

$ - $

Equal Opportunity Employer

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law.

Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

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Position Requirements
10+ Years work experience
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