Associate Director of Statistical Programming
About The Position
Recursion is at the forefront of reimagining drug discovery through the integration of automated cell biology, high-dimensional and diverse data sets, and sophisticated analytics. We are seeking an experienced Senior Manager/Associate Director of Statistical Programming to provide Statistical Programming leadership and expertise in support of clinical development, including oversight of vendors and contract programmers to ensure quality deliverables, and to validate results. In this role, you will: Lead statistical programming activities across clinical programs, ensuring the development and quality control of tables, listings, figures, analysis datasets. Conduct exploratory statistical analysis to support key decision-making Oversee external functional service providers to ensure timely and high-quality programming deliverables Develop and maintain standards, guidance, applications, and processes for Statistical Programming operations in adherence with ICH and regulatory requirements Drive the adoption of innovative programming technologies and workflows to enhance the efficiency of clinical data review, cleaning, reconciliation, and integration. Additionally, develop analytics tools that enable effective data monitoring and knowledge discovery of clinical data As Senior Manager/Associate Director of Statistical Programming, you'll report directly to the Head of Statistical Programming and will be a key member of the Biometrics Leadership Team. The Biometrics Team is an innovation-driven and execution-minded group of drug development professionals responsible for supporting Recursion's innovative science through novel trial design, data collection, integration, analysis, and enabling data-driven decision making.
Requirements
- BS/MS degree in life science, computer science, statistics, mathematics, or equivalent relevant degree.
- 8+ years of statistics and programming experience with advanced knowledge in pharmaceutical, biotechnology industries, and 5+ years of serving as Lead Statistical Programmer across multiple therapeutic areas.
- Demonstrated proficiency in SAS, R, and R-Shiny and mastery of complex graphing techniques to derive analysis datasets, produce tables, figures and listings, and conduct exploratory analyses.
- Expert knowledge of data standards including CDISC, SDTM, and ADaM, and relevant regulatory guidelines.
- Experience with regulatory submissions in the US, Europe, and other regions.
- Excellent interpersonal and communications skills including ability of conflict management and resolution.
Nice To Haves
- Skilled in developing open-source R packages and visual analytics for exploratory and interactive data analysis, visualization, and insight generation.
Responsibilities
- Lead statistical programming activities across clinical programs, ensuring the development and quality control of tables, listings, figures, analysis datasets.
- Conduct exploratory statistical analysis to support key decision-making
- Oversee external functional service providers to ensure timely and high-quality programming deliverables
- Develop and maintain standards, guidance, applications, and processes for Statistical Programming operations in adherence with ICH and regulatory requirements
- Drive the adoption of innovative programming technologies and workflows to enhance the efficiency of clinical data review, cleaning, reconciliation, and integration.
- Develop analytics tools that enable effective data monitoring and knowledge discovery of clinical data
Benefits
- You will also be eligible for an annual bonus and equity compensation, as well as a comprehensive benefits package.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
