Senior Medical Writer I

Eikon Therapeutics • Jersey City, NJ

1d • $125,000 - $136,800 • Hybrid

About The Position

Eikon Therapeutics is seeking an experienced, detail-oriented individual to join its Medical Writing team. In the Senior Medical Writer I role, the individual will be responsible for independently leading document development by authoring and editing medical and regulatory writing deliverables that support the Eikon clinical portfolio. This role requires partnering with cross-functional colleagues within study teams/project teams to prepare high-quality, accurate, and fit-for-use clinical and regulatory documents, enabling the delivery of Eikon portfolio milestones. This role will require a minimum of 3 days a week of onsite presence in either Jersey City (NJ) or Millbrae (CA) offices.

Requirements

• Doctoral-level degree in Life Sciences (e.g., Ph.D., M.D., PharmD; preferred), or Master’s degree with 3+ years of relevant experience, or Bachelor’s degree with 5+ years of relevant experience in regulatory, scientific, or medical writing.
• Substantial clinical study protocol writing experience desired.
• Excellent communication, presentation, and project management skills.
• Ability to independently prepare clinical and regulatory documents (e.g., protocol, CSR, IB, CTD modules) in compliance with company SOPs and international health agencies/regulatory guidelines with a focus objective data presentation in a clear, concise format in keeping with industry guidelines.
• Working knowledge of statistical concepts and techniques.
• Proven track record of meeting project timelines/deliverables and attention to detail, process, deadlines, and high-quality results.
• Strong understanding of federal regulations, GCPs, and ICH guidelines is a plus.
• Understanding of clinical development, including study phases, submission processes, and techniques used within a clinical development environment from protocol design through regulatory submission and support for marketed products.
• Technical expertise in typical office applications (e.g., Microsoft Office, Adobe Acrobat) shared document systems (e.g., SharePoint, Veeva RIM, PleaseReview), and with specialized software (e.g., GraphPad Prism, PerfectIt, SmartSheet, Endnote).
• Familiarity with concepts of structured content management preferred.
• Proven ability to work independently in a dynamic, fast-moving environment while striving for excellence in collaboration and innovation, as part of a cross-functional team.

Nice To Haves

• Strong understanding of federal regulations, GCPs, and ICH guidelines is a plus.
• Familiarity with concepts of structured content management preferred.

Responsibilities

• Independently write clinical and regulatory documents, including (but not limited to): clinical protocols, clinical study reports (CSRs), investigator brochures (IBs), common technical document (CTD) modules (Module 2.7.Xs, 2.5, and Module 5 integrated summaries), briefing documents, posters, abstracts, manuscripts and other documents per company and regulatory guidelines.
• Interpret data and apply knowledge of regulatory/compliance/scientific requirements to document preparation.
• Independently manage and maintain document lifecycle, including timelines, workflow of writing assignments, review cycle management, and document quality management where appropriate.
• Help to iteratively improve medical writing processes as appropriate.
• Contribute to document quality control (QC) as needed and help ensure consistency across documents to ensure adherence to company style and regulatory agency expectations.
• Take ownership of a given assignment, proactively consulting other cross-functional project team members to align and build consensus on timelines, document interdependencies, organize and drive kick off meetings, comment resolution meetings, and ad-hoc meetings to mitigate risks and resolve project related issues.
• Interpret and understand scientific and clinical data, provide input on data, figures, tables, and listings for clear data presentation per the document scope.

Benefits

• 401k plan with company matching
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
• Mental health and wellness benefits
• Weeklong summer and winter holiday shutdowns
• Generous paid time off and holiday policies
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies
• Enhanced parental leave benefit
• Daily subsidized lunch program when on-site

What This Job Offers

• Job Type: Full-time
• Career Level: Senior