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Eikon Therapeutics

Associate Director, Biostatistics

Posted 15 Days Ago
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In-Office
Jersey City, NJ
Senior level
In-Office
Jersey City, NJ
Senior level
The Associate Director, Biostatistics will lead statistical efforts in clinical trials, guide teams, and mentor biostatisticians while ensuring regulatory compliance and employing advanced statistical methodologies.
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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.

Position

We are seeking a skilled and highly motivated Associate Director, Biostatistics to join our talented team. The successful candidate will contribute their statistical expertise and strategic thinking to the design, execution, and analysis of clinical trials and experimental studies. In collaboration with cross-functional teams, you will lead statistical efforts that facilitate evidence-based conclusions and guide our research and development initiatives.

This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in our New Jersey office to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration.  

About You

The ideal candidate for this role should possess a proven track record of designing and analyzing clinical trials and experimental studies, particularly within the biotechnology, pharmaceutical, or related industries. This candidate excels in leading interdisciplinary teams to design studies, developing statistical analysis plans, performing advanced statistical analyses, and providing guidance to team members. Their proficiency in statistical programming languages, understanding of regulatory guidelines, and excellent communication skills are essential for conveying complex statistical concepts to non-technical stakeholders. The ideal candidate also demonstrates leadership capabilities and a deep knowledge of emerging trends and best practices in biostatistics, statistical tools, and software.

What You’ll Do

  • Collaborate with interdisciplinary teams to design clinical trials, experiments, and studies, ensuring appropriate statistical methodologies are employed.
  • Lead the development of statistical analysis plans, including endpoints, sample size determination, randomization strategies, and statistical methodologies.
  • Perform advanced statistical analyses on complex datasets, interpreting results and drawing actionable conclusions.
  • Provide guidance and mentorship to biostatisticians and statistical programmers within the team.
  • Contribute to regulatory submissions by providing statistical expertise and preparing relevant sections of documents.
  • Stay current with emerging trends and best practices in biostatistics and their application in the biotechnology field.
  • Drive the implementation and utilization of advanced statistical tools and software.

Qualifications

  • PhD or equivalent degree in statistics/biostatistics or related discipline with a minimum of 6 years of clinical research and drug development experience.
  • Proficiency in statistical programming languages (e.g., R, SAS) and experience with data visualization tools.
  • Strong understanding of regulatory guidelines (ICH, FDA, etc.) and their implications on statistical analysis and reporting.
  • Experience in authoring statistical analysis plans and performing statistical analyses and reporting using tables, listings, and figures. Oncology experience is a plus.
  • Excellent communication skills with the ability to convey complex statistical concepts to non-technical stakeholders.
  • Demonstrated leadership capabilities, including the ability to lead and mentor a team.
  • Experience with Bayesian statistics and adaptive trial designs.
  • Publications in peer-reviewed journals showcasing contributions to the field of biostatistics.

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 $200,000 to $218,500 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.

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