What are the responsibilities and job description for the Eikon Therapeutics, Inc. is hiring : Associate Director, Medical Writing in New Y position at Eikon Therapeutics, Inc.?
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Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real-time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.
Please note that starting April 2025, Eikon Hayward positions will be moving to our new headquarters in Millbrae, CA.
Position
We are seeking an experienced, detail-oriented individual to work with our Medical Writing team. In the Senior Medical Writer role, you will be responsible for independent lead authoring and editing of medical and regulatory writing deliverables that support the clinical portfolio. You will partner with colleagues within Medical Writing as well as with the Nonclinical, Clinical, & Regulatory teams to prepare high-quality, accurate, and concise documentation supporting the objectives of both teams and leadership.
This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our Jersey City (NJ), New York (NY), or Millbrae (CA) offices to ensure effective management, operational excellence, and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration.
About You
You are an experienced, independent, scientifically minded individual with a passion for accurate and concise medical and regulatory writing.
What You’ll Do
- Independently author regulatory documents, including (but not limited to) : clinical protocols, clinical study reports (CSRs), investigator brochures (IBs), common technical document (CTD) modules, briefing documents, and other nonclinical or clinical documents per company and regulatory guidelines.
- Contribute to document development as an independent lead author and as part of a larger team.
- Interpret data and apply knowledge of regulatory / compliance / scientific requirements to document preparation.
- Independently manage document lifecycle, including timeline management, 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.
Qualifications
At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including :
The expected salary range for this role is $174,000 to $190,000 depending on skills, competency, and the market demand for your expertise.
Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment.
We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees, or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.
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Salary : $174,000 - $190,000
