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 Director of Statistical Programming, the Associate Director/Senior Manager, Statistical Programming will support oncology drug development, providing programming expertise and oversight to the clinical development. 

 

Key Responsibilities:


·         Lead SAS programming activities, to the agreed timeline, budget, and quality in accordance with Company study contacts and SOPs

·         Works with biostatisticians, develops data specs, analysis datasets and analysis outputs per requests for internal medical monitoring, CSR and submission need

·         Works with data managers, generates ongoing outputs to support data cleaning and enhance data integrity

·         Provides programming expertise to review/QC the programming work provided by CRO, including timeline along with QC outputs, datasets, and programming related documents, and debugging programming errors

·         Through oversight and effective delegation, ensure SAS Programming activities on assigned studies are completed accordingly within the scope of the study contract and manage progress against the study contract and project plan, driving all Programming activities to their conclusion while maintaining accurate resource forecasts. Lead study team members, providing study specific training and guidance where appropriate

·         Develop SOP for Statistical Programming with collaboration with cross-functional teams

·         Develops, manages, and maintains analysis data and reporting deliverables. Ensures timely, targeted, and accurate reporting and outcomes

·         Ability to work within a team and work independently

 

Education and Experience:


·         Bachelor’s Degree in statistics, computer science or another related science field with a minimum of 6 years (10 years for Associate Director) 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 4 years (8 years for Associate Director) 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

·         Excellent organizational skills and good verbal and written communication skills

·         Ability to work independently as well as lead programming teams

·         Strong communication skill set with peers, business partners, and Sponsors

·         Leadership skills to lead project team to deliver high quality deliverables on time and work directly with the Sponsor to meet the project delivery expectations

 

 

Salary Range: 

Senior Manager or Associate Director $145,000-$190,000 DOE 

 


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.

 

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