Skip to main content
Tallo logoTallo logo

Senior Medical Writer II

Job

Eikon Therapeutics

Jersey City, NJ (In Person)

$154,750 Salary, Full-Time

Posted 6 weeks ago (Updated 1 day ago) • Actively hiring

Expires 6/22/2026

Apply for this opportunity

This job application is on an outside website. Be sure to review the job posting there to verify it's the same.

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
75
out of 100
Average of individual scores

Were these scores useful?

Skill Insights

Compare your current skills to what this opportunity needs—we'll show you what you already have and what could strengthen your application.

Job Description

Senior Medical Writer II Eikon Therapeutics Marketing & Communications Jersey City, NJ, USA USD 148k-161,500 / year + Equity Posted on Apr 11, 2026 Apply now 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. Position As a Senior Medical Writer 2, you will play a pivotal role in translating complex scientific and medical information into clear and concise written materials. Operating in a dynamic and collaborative environment, you will contribute to the development of various documents that support our research, clinical trials, and regulatory activities. About You The ideal candidate for this position should possess strong writing and communication skills, with the ability to effectively convey complex scientific concepts in a clear and concise manner. Exceptional attention to detail and a commitment to producing accurate and high-quality written materials are essential. Proficiency in Microsoft Office Suite and familiarity with scientific writing tools is important, and the candidate should be capable of thriving in a fast-paced and collaborative work environment. While knowledge of clinical research, regulatory requirements, and biotechnology is advantageous, it is not required.
What You'll Do Document Preparation:
Create a wide range of medical and scientific documents, including clinical study protocols, investigator brochures, regulatory submissions, and scientific publications.
Content Development:
Collaborate closely with cross-functional teams to collect and interpret data, ensuring accuracy and relevance in written materials.
Regulatory Compliance:
Ensure that all written materials strictly adhere to regulatory guidelines, industry standards, and internal quality standards.
Literature Review:
Conduct comprehensive literature reviews to support the development of evidence-based documents.
Data Interpretation:
Proficiently interpret and summarize complex scientific data and clinical trial results for various audiences.
Editing and Proofreading:
Review and edit documents for grammar, clarity, and consistency while maintaining a high level of accuracy.
Collaboration:
Collaborate closely with scientists, clinical teams, and regulatory affairs professionals to align written materials with project goals and timelines.
Mentorship:
Provide guidance and mentorship to junior medical writers, fostering their professional growth and development. Qualifications PhD with 3 years of experience or a Master's degree with 6 years of experience or a Bachelor's degree with 8 years of experience in a relevant field (e.g., life sciences, healthcare, or related discipline). Strong writing and communication skills, with the ability to effectively convey complex scientific concepts in a clear and concise manner. Exceptional attention to detail and commitment to producing accurate and high-quality written materials. Proficiency in Microsoft Office Suite and familiarity with scientific writing tools. Capability to thrive in a fast-paced and collaborative work environment. Knowledge of clinical research, regulatory requirements, and biotechnology is advantageous but not required. At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​ 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​ The expected salary range for this role is $148,000 to $161,500 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. Apply now See more open positions at Eikon Therapeutics

Similar jobs in Jersey City, NJ

Similar jobs in New Jersey