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Senior Medical Writer

10 May 5, 2025
Job Description
Job Type: Hybrid Education: PharmD, Ph.D, Master in science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title: Senior Medical Writer

Company: Eikon Therapeutics
Location: Jersey City, NJ; New York City, NY; Millbrae, CA (Hybrid – minimum 3 days onsite/week)


Job Type: Full-time

Salary Range: $125,000 – $136,800 (plus bonus & equity)


About the Company

Eikon Therapeutics is a pioneering biopharma company utilizing Nobel Prize-winning single-molecule imaging to develop breakthrough therapies by directly visualizing protein dynamics in living cells.


Role Summary

As Senior Medical Writer, you will lead the development of clinical and regulatory documents across Eikon’s drug development portfolio. You will work cross-functionally with clinical, regulatory, and scientific teams to produce high-quality, fit-for-purpose documentation that supports study execution and regulatory submissions.


Key Responsibilities

  • Independently write and edit clinical documents: protocols, CSRs, IBs, CTD modules, briefing documents, abstracts, and manuscripts

  • Interpret scientific and clinical data; present information in clear, concise, compliant formats

  • Manage document timelines, review workflows, and quality control

  • Drive document-related meetings and collaborate closely with study teams

  • Ensure consistency across deliverables and alignment with health authority expectations

  • Contribute to continuous improvement of writing processes and templates


Qualifications

  • Doctoral degree (Ph.D., M.D., PharmD) preferred; Master’s + 3 years or Bachelor’s + 5 years of relevant experience considered

  • Strong experience writing clinical protocols and other regulatory documents

  • Working knowledge of GCP, ICH guidelines, and clinical development lifecycle

  • Proficient in MS Office, Adobe Acrobat, and systems like SharePoint, Veeva RIM, PleaseReview

  • Familiarity with structured content management, GraphPad Prism, PerfectIt, and Endnote preferred

  • Strong communication and organizational skills with ability to manage multiple projects independently


Compensation & Benefits

  • Competitive base salary with performance bonus and equity options

  • 401(k) with company match

  • Medical (95%), dental & vision (100%) premiums covered

  • Mental health and wellness programs

  • Summer and winter week-long shutdowns

  • Generous PTO and holiday plan

  • Enhanced parental leave

  • Life/AD&D insurance (100% company-paid)

  • Daily subsidized lunch onsite


Diversity & Inclusion

Eikon is committed to diversity and equal opportunity in hiring. All qualified candidates will be considered regardless of background.