Skip to content
×

Medical Writer; Pharmaceutical) remote

Remote / Online - Candidates ideally in
Schenectady, Schenectady County, New York, 12301, USA
Listing for: Executive Staff Recruiters / ESR Healthcare
Remote/Work from Home position Listed on 2026-11-05
Job specializations:
Salary/Wage Range or Industry Benchmark: 90000 - 135000 USD Yearly USD 90000.00 135000.00 YEAR

Job Description & How to Apply Below

Position: Medical Writer (Pharmaceutical) remote
Job Description

Medical Writer (Pharmaceutical)

(Use the "Apply for this Job" box below)..micro
1.ai/post/6da7a95c-8ab7-4b76-a835-?referral

Code=10002f4f-2f65-476f-b8d5-434a&=referral&=share&=

Role Type:
Contractor

Location:

Remote

Scope of Work
  • Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs, and related clinical documents to inform AI tool development.
  • Apply expert judgment to assess whether AI-generated content fulfills clinical template and structural requirements, including ICH E3 organization, section sequencing, cross-referencing, and appendix management.
  • Evaluate scientific accuracy in narrative sections such as efficacy, safety summaries, discussion, and conclusions, distinguishing true scientific or interpretive errors from stylistic differences.
  • Trace narrative claims to source records-tables, figures, listings, and protocols-to verify that all assertions are appropriately supported.
  • Provide clear and structured written rationales for each assessment, enabling precise diagnosis and improvement of AI model behavior.
  • Collaborate with project leads to refine evaluation frameworks and document best practices for clinical regulatory writing in the context of AI.
    • Preferred Qualifications
  • Minimum 5 years of regulatory medical writing experience at a sponsor, CRO, or as an independent consultant.
  • Direct experience independently authoring or leading the authoring of full Clinical Study Reports, beyond summaries or partial contributions.
  • Fluency with ICH E3 and conventions for periodic safety documentation (ICH E2F, ICH E2C) and eCTD placement.
  • Demonstrated ability to read and interpret TFLs and protocol documents, identifying where narrative diverges from source data.
  • Exceptional written and verbal communication skills, especially in providing structured, actionable feedback on clinical content.
  • Advanced degree in life sciences, pharmacy, or medicine (PhD, PharmD, MD, MSc), or equivalent depth of authoring experience.
  • Experience across multiple clinical phases and therapeutic areas; oncology and haematology expertise is especially valued.

    • Join our customer's team and leverage your authoring expertise to help design the next generation of AI-assisted clinical documentation solutions. This high-bar role offers you the chance to shape how tomorrow's writing teams draft and review regulatory documents - through your expert input, judgment, and real-world experience.

    Working Place

    NYC, New York, United States

    Company

    ESR Healthcare

    To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
    (If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
    View / Apply for Jobs
    Matching My Jurisdiction

    Search for further Jobs Here:

    SEARCH JOBS: 10+ Million Listings
    (Try combinations for better Results! Or enter less keywords for broader Results)
    Education Level
    Experience Level (years)
    Posted in last:
    Salary