Data Systems & Clinical Programming Specialist (Contractor)
Company: Alumis Inc.
Location: South San Francisco
Posted on: March 2, 2026
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Job Description:
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 Data
Systems & Clinical Programming Specialist (Contractor) will be
responsible to support Data Management (DM) as part of the Clinical
Programming function in a rapidly evolving environment, in
accordance with industry standards. This role will support Data
Systems and Clinical Programming activities and deliverables across
programs as directed by the Director and Associate Director,
DS&CP. Essential Responsibilities: Support development and
production operation activities within the Data Systems and
Clinical Programming function Maintain Smartsheet trackers for
report requests, Production reports, and other DS&CP
operational documentation Participate in the development of report
specifications for SAS Clinical Programming reports, and other
custom reports/outputs as needed Review programmed reports/outputs
for accuracy against requirements and provided specifications
Provide/transfer source files for reports and dashboards and ensure
automated transfers have completed successfully Transfer programmed
reports/outputs to appropriate locations for cross-functional team
use Support requests for new/updated Automated Transfer Service
(ATS) vendors and jobs and investigate issues or trigger jobs
manually as needed Provide user access for DM tools Support Alumis’
standard CRFs and standard edit checks initiatives Participate in
EDC, IRT, and eCOA User Acceptance Testing (UAT) Ensure DS&CP
study-specific documentation is in an inspection-ready Support
DS&CP in cross-functional meetings, as applicable Ensure
DS&CP project deliverables are completed on time and in
accordance with quality standards and regulatory requirements
Ensure compliance with all relevant data privacy regulations and
maintain the security of clinical trial data Qualifications: 5
years of relevant experience and has earned a BS or equivalent
degree 2 years of experience with clinical trials and data
management Understanding of the programming development life cycle
Knowledge and experience in EDC Experience with SAS, SQL, and/or
other clinical programming tools Experience working and effectively
communicating with global programming teams preferred Experience
with CDISC standards (CDASH, SDTM) preferred Strong interpersonal,
organizational, and communication (oral and written) skills Logical
thinking, attention to detail and accuracy, strong organizational
skills, and problem-solving abilities Ability to prioritize and to
adapt quickly to changing business conditions with a “can-do”
attitude
Keywords: Alumis Inc., Daly City , Data Systems & Clinical Programming Specialist (Contractor), Science, Research & Development , South San Francisco, California
