Associate Director, Statistical Programming
Needham, MA, United States23h ago
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Key details
- Salary
- $154K–$200K/yr
- Location
- Needham, MA, United States
- Work style
- Onsite
- Level
- Lead / Staff+
- Experience
- 8–11 yrs
- Function
- Operations & Strategy
- Focus area
- other
- Posted
- 23h ago
Skills
data structuresquality controlrsassqlstatistical analysis
About the role
Overview
This role at Celldex Therapeutics is a senior-level leadership position focused on overseeing the end-to-end statistical programming lifecycle. It combines technical oversight, project management, and cross-functional collaboration to ensure clinical trial data meets rigorous regulatory standards.
Responsibilities
- Lead or Co-ordinate statistical programming activities of all programmers either internally or externally assigned to the study/project work, mentor other programmers in functional expertise and processes. Make statistical programming decisions/recommendations at study or project level.
- Comply with company, department and industry standards (e.g. CDISC) and processes, responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results.
- Oversee the creation of CDISC compliant submission readiness output including but not limited to datasets (SDTM, ADaM), Tables, Listings and Figures (TFLs) and associated Define packages.
- Oversee the external programming activities outsourced to CROs to ensure the quality including standard programming practice, validation, and documentation.
- Build and maintain effective working relationships with cross-functional teams both internally and externally, contribute to the status of deliverables and critical programming aspects (timelines, scope, resource plan etc.)
- Support all in-house programming activities, if needed, including but not limited to regulatory filings, adhoc analysis, publication requests etc.
Qualifications
- MS in Statistics or related field
- 8+ years of SAS programming experience in the biotech/pharma industry
- Experience as the lead programmer coordinating programming teams to support multiple regulatory submissions
- Experience managing people and projects.
- Proficiency with SAS Base, Macro, SQL, and Graph; working knowledge of R is a plus.
- Experience working with and managing external CROs or FSPs for programming deliverables.
- Familiarity with CDISC (SDTM/ADaM) standards and ability to adapt them for non-interventional data structures.
- Excellent communication skills and ability to work cross-functionally in a lean team environment.