Senior Manager, Statistical Programming at Eikon Therapeutics

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

The Senior Manager of Statistical Programming will be accountable for statistical programming deliverables in Eikon clinical studies. In this role, you will report to the Sr. Director of Statistical Programming. This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our California, New York or New Jersey 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 will oversee and manage the statistical programming deliverables for clinical studies, ensuring that they meet quality, compliance, and timeliness requirements. The role requires collaboration with various stakeholders, including Biostatistics, Clinical Research, Regulatory, Clinical Safety, Data Management, and PK/PD Modeling.

What You’ll Do

• Be responsible for statistical programming deliverables in multi-disciplinary interactions
• Provide development, review and approval for statistical programming documents, oversight vendor programming work to ensure high quality as well as operational excellence
• Have In-depth understanding of CDISC standards (SDTM, ADaM, Define.xml, etc.) and apply corresponding knowledge to develop ADaM specifications, SAS programs and review regulatory electronic submission packages
• Conduct statistical programming and/or statistical simulations to support clinical decision making, regulatory interaction, and publications
• Support statistical programming quality control process and develop functional Standard Operating Procedures (SOPs) and Work Instructions
• Support the development of CRFs, edit checks, review of Data Transfer Specifications, and any other collaborations with Data Management function

Qualifications

• Post Graduate degree with 6+ years of experience or a Bachelor's degree with 8+ years of experience in a relevant field (e.g., statistics, biostatistics, computer science, or a related discipline). 
• Expertise in SAS and clinical trial programming; Experience in R is a plus
• Superior knowledge and significant experience in setting strategy and developing analysis and reporting statistical programming deliverables (datasets, statistical analyses, report tables, and graphics) using global and TA standards based on quality, compliance and timeliness requirements
• US of worldwide drug regulatory application submission experience including the development of electronic submission deliverables
• Experience in CDISC and ADaM standards
• Demonstrated success in the assurance of deliverable quality and process compliance
• Excellent interpersonal skills and ability to negotiate and collaborate effectively
• Recent experience working in the field of oncology preferred but not required
• Experience developing and implementing statistical programming standards preferred but not required
• Experience developing JReview reports to support medical monitoring preferred but not required
• Strong working knowledge of reporting processes (e.g., SOPs) and statistical computing environments preferred 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 $157,000 to $171,000 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.

In accordance with the Company’s duty to provide and maintain a safe workplace, the Company requires all employees to be Fully Vaccinated with one of the FDA approved COVID-19 vaccines, which includes those vaccines that have received the FDA’s emergency use authorization. You will be expected to be Fully Vaccinated as of your Start Date. If you believe that you are exempt from this requirement under an applicable law or regulations, including Americans with Disabilities Act and California’s Fair Employment and Housing Act, you will need to contact the Company’s Human Resources group. For purposes of this section, Fully Vaccinated means (i) the completion of the vaccination regimen as approved by the FDA (by way of example, 2 doses of the Pfizer or Moderna vaccine and 1 dose of the Johnson and Johnson vaccine), and (ii) timely receiving booster vaccination, as recommended by the Centers for Disease Control and Prevention.

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.