Principal Statistical Programmer - ALX Oncology Inc.

ALX Oncology is a clinical-stage and patient-focused immuno-oncology company developing therapies that block the CD47 myeloid checkpoint pathway. Our lead candidate, evorpacept (ALX148), is a next generation CD47 blocking therapeutic that combines a high-affinity CD47 binding domain with an inactivated proprietary Fc domain. For more information about us, please visit www.alxoncology.com.

Reporting to the Associate Director of Statistical Programming, the Principal Statistical Programmer will provide programming support and expertise to our clinical development programs.  

Key Responsibilities and Success Factors:

• Perform SAS programming activities to meet timelines, budget, and quality in accordance with Company study contracts and SOPs

• Effectively work with Biostatisticians and Statistical Programming team to review data specs, generate or QC analysis datasets and generate or         QC analysis outputs per requests for internal medical monitoring, CSR and submission needs

 • Work with data managers to generate ongoing outputs to support data cleaning and to enhance data integrity

 • Communicate effectively within Biometrics and with cross-functional team members

 • Provide programming expertise to review/QC the programming work provided by the CRO including QC outputs, datasets, and programming            related documents; debug programming errors as needed

 • Work on special projects as needed

 • Support internal analysis data and reporting deliverables. Ensure timely, targeted, and accurate reporting and outcomes.

 • Develop or QC and document Statistical Programming team macros

 • Ability to work within a team as well as independently

 • Ability to lead a programming deliverable as needed

Education and Experience:

 • Bachelor’s Degree in statistics, computer science or another related science field with a minimum of 10 years of SAS programming experience          with clinical trial data OR master’s degree in statistics, computer science or another related science field with a minimum of 8 years of SAS                programming experience with clinical trial data

• Good working knowledge of CDISC SDTM and ADaM Implementation Guidelines

• General knowledge of regulatory requirements and drug development process

• Strong verbal and written communication skills

• Ability to work independently as well as part of programming teams

• Strong communication skill set with peers and other group partners

• Consistently deliver high quality deliverables on time and meet the project delivery expectations

Hybrid work model acceptable (i.e., part-time in South San Francisco office with flexibility to work part-time from home)

Salary: $156,706-$176,485

ALX Oncology is an equal opportunity employer. All applicants should be legally entitled to work for any employer in the US. Title and salary are commensurate with experience. Our compensation program includes competitive salary, equity participation and attractive bonus incentives.