Skip to main content

This job has expired

You will need to login before you can apply for a job.

Director, Statistical Programming

Employer
Alumis Inc.
Location
South San Francisco
Start date
Oct 25, 2024
View more categoriesView less categories
Discipline
Information Technology, Bioinformatics
Required Education
Bachelors Degree
Position Type
Full time
Hotbed
Biotech Bay

Job Details

Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients. 

Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer - our goal is to fundamentally change the outcomes for these patients.   

 

We are seeking an experienced Statistical Programming Director who will be primarily responsible for overseeing statistical programming activities in a drug development program and ensuring programming activities in compliance with SOPs and regulatory requirements to produce quality and timely deliverables.

 

Responsibilities
  • Lead statistical programming for study/indication; represent the statistical programming team at Study Execution Team and Clinical Development Team to address deliverables and timelines.
  • Contribute to strategies for programming-related matters in submission to regulatory agencies, publications and other communications as needed.
  • Provide technical leadership and guidance to programming team and vendors on conventions, best practices, standards, specifications, and solutions to complex programming tasks.
  • Interact and communicate with Statisticians, Data Managers, Clinical Operations, Medical Monitors, Medical Writing and Medical Monitors to address programming related study deliverables.
  • Participate in the review of key study-related documents produced by other functions, e.g. SAP, case report form, data management plan, database specifications, EDC data structures, DMC plans, and other clinical documents.
  • Lead/contribute to departmental process and standards initiatives such as the development of processes and CDISC standards.
  • Develop product- and study-level macros and utilities to improve programming efficiency.
  • Oversee CRO programming activities; review and validate deliverables produced by CROs, independently provide solutions to issues raised by CROs.
  • Conduct ad-hoc analysis requests, data validation, etc. in accordance with all relevant statistical regulatory guidance and standards.
  • Advanced knowledge of submission requirements and standards; ensure statistical programming activities are in compliance with regulatory requirements, industry and company standards; accountable for quality deliverables.

 

The Ideal Candidate
  • Expert level SAS programmer with experience in delivering complex programming assignments and analysis. Proficient in developing their own code including macros as well as modifying existing code.
  • Experience in development and implementation of statistical programming standards and procedures
  • Expert-level knowledge and extensive hands-on experience with CDISC standards such as CDASH, SDTM, and ADaM
  • Experience leading teams supporting FDA/EMEA/CDE filings.
  • Strong interpersonal and effective communication (oral and written) skills.
  • Thorough and strong attention to detail and consistency

 

Education

Bachelor’s degree or equivalent education, preferably in a computational or biological science, with a minimum of 12 years of directly related experience in a drug development environment. Or Master’s degree with a minimum of 10 years of related experience.

 

The salary range for this position is $220,000 USD to $234,000 USD annually. This salary range is an estimate, and the actual salary may vary based on the Company’s compensation practices.   

This position is located in South San Francisco, CA and employees are expected to be onsite Tuesday-Thursday.*  At this time we are not considering remote applicants.

Alumis Inc. is an equal opportunity employer.

Alumis compensation packages include generous stock option grants for all employees as well as an annual bonus program.  

Other benefits include:

  • Health insurance premiums paid at 90% for employee, 80% for dependents
  • Free access to Genentech Bus & Ferry Share program
  • $100 monthly cell phone stipend
  • Unlimited PTO for Exempt employees
  • Free onsite gym and a kitchen stocked with yummy snacks and drinks!

We are a hard-working, collaborative team on a mission to transform patient’s lives-- and we aspire to elevate, challenge and nurture one another along the way.

*Alumis Lab personnel are generally onsite 4-5 days/week 

Company

Alumis Inc. is a precision medicines company with the mission to transform the lives of patients with autoimmune diseases. Our experienced leadership team brings a proven track record in precision drug development of groundbreaking therapies.

Even with treatment innovations of the last two decades, many patients with immunologic conditions continue to suffer.

With a unique precision analytics platform and an unwavering commitment to advancing our understanding of immunologic diseases, Alumis Inc. will rewrite the autoimmune treatment playbook by developing the right medicine for each patient.
 

Company info
Website
Location
611 Gateway Blvd
Suite 820
South San Francisco
California
94080
US

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert