Senior Manager, Statistical Programming

Alumis•South San Francisco, CA

9h•Onsite

About The Position

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 Senior Manager, Statistical Programming to drive the development and validation of statistical programs for late-stage clinical studies. In this role, you will ensure programming activities align with SOPs and regulatory requirements, delivering high-quality and timely results. This is an exciting opportunity to contribute to critical drug development efforts while driving efficiency and compliance in statistical programming.

Requirements

Expert-level SAS programmer with a proven track-record of delivering complex programming assignments and analyses.
Skilled in writing original cold, developing macros and modifying existing code.
Experience in developing and implementing statistical programming standards and procedures.
Expert level knowledge and extensive hands-on experience with CDISC standards including CDASH, SDTM, and ADaM.
Experience leading teams supporting FDA, EMEA, and CDE regulatory filings.
Strong interpersonal skills with excellent written and verbal communication.
Meticulous attention to detail and consistency.
Bachelor’s degree (or equivalent), preferably in a computational or biological science, with a minimum of 8 years of direct experience in drug development.
Master’s degree with minimum of 6 years of related experience.

Responsibilities

Lead the development and validation of statistical programs to ensure high-quality deliverables for both in-house and outsourced projects, adhering to company and regulatory requirements.
Drive ISS/ISE analysis tasks in support of NDA submissions.
Assist in planning and coordinating project work to ensure timely and high-quality delivery across multiple studies.
Develop and review programming plans, dataset specifications, and TLFs; apply expertise in CDISC standards, including SDTM and ADaM models.
Review documents produced by biometric functions such as SAPs, CRFs, data review plans, and data transfer agreements.
Oversee CRO programming activities, reviewing and validating CRO deliverables including SDTM, ADaM and TLFs, while providing solutions to any issues raised by CROs.
Review eSubmission datasets and data documentation such as aCRF, reviewer guides, define documents and programs to ensure all files meet submission requirements.
Develop macros to support study and project activities, contributing to global macro tools that enhance the overall efficiency and capacity of the programming function.
Maintain deep familiarity with ICH guidelines and advanced knowledge of regulatory submission requirements, ensuring all statistical programming deliverables meet industry and company standards.
Support the preparation of clinical study reports, regulatory submissions, DSURs, and safety reports across multiple studies.
Contribute to the development, implementation and continuous improvement of programming processes and standards.
Communicate effectively within project teams, across departments, and with external collaborators.