What are the responsibilities and job description for the Director, Biostatistics position at Alumis Inc.?
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.
The Associate Director of Biostatistics will play a key role in providing statistical leadership across multiple Phase 2 and 3 clinical trials. As the statistical lead, you will develop and oversee statistical analysis plans, ensure the quality and accuracy of deliverables, and manage CRO partners to meet project timelines and standards. This role requires expertise in simulation work, multiple imputation analyses, and late-phase clinical development.
As the Director of Biostatistics at Alumis, you will join a high-performing team of experienced drug developers dedicated to transforming outcomes for patients with autoimmune diseases. We are seeking someone with substantial filing knowledge and hands-on experience to play a critical role in the execution of the development of our lead compound. You will oversee the quality and accuracy of statistical analyses, and collaborate cross-functionally to develop integrated analyses for regulatory submissions. This role involves hands-on contributions to key statistical deliverables, such as analysis plans, clinical study reports, and data packages for regulatory submissions, while managing CROs and mentoring junior team members. Guided by our core values—We Elevate, We Challenge, We Nurture—you will play a pivotal role in advancing innovative therapies alongside a talented and experienced team.
Essential Responsibilities :
- Apply advanced statistical methods to clinical trial data summaries and interpretations including integrated safety and efficacy analyses to support regulatory submissions.
- Provide statistical input for drug development plans, clinical study design, and operationalization.
- Perform as study statistician including the development or review of statistical analysis plans, clinical study reports, and presentations.
- Manage and oversee CROs.
- Ensure the quality and accuracy of study data and statistical outputs.
- Perform quality control checks on key efficacy and safety endpoints to validate data.
- Mentor junior staff and contractors, while primarily serving as an individual contributor.
The Ideal Candidate :
Education :
Experience :
Skills :
The salary range for this position is $245,000 USD to $255,000 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.
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 :
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.
Salary : $245,000 - $255,000
