Job Overview
Location
Remote, USA
Job Type
Full-time
Category
Data & Analytics
Date Posted
April 24, 2026
Full Job Description
đź“‹ Description
- • The Associate Director, Statistical Programming leads and oversees statistical programming activities for internal and external teams, ensuring deliverables comply with company SOPs and ICH/GCP standards while managing a drug program team of statistical programmers to accomplish tasks and communicate issues to senior management.
- • Day-to-day responsibilities include leading the creation, oversight, review, completion, and delivery of statistical programming deliverables; providing expertise in CDISC SDTM and ADaM implementation; authoring analysis dataset specifications; managing end-to-end programming from CRF collection to electronic submission; identifying process inefficiencies and leading improvement efforts; serving as the Statistical Programming Lead to achieve milestones; verifying consistency of data, analysis, and submission standards; and aligning internal and external teams on requirements and resource needs.
- • Biogen is a global biotechnology company focused on finding therapies for neurological and rare diseases, operating with a mission-driven culture that values collaboration, scientific rigor, and resilience, where employees work together to overcome obstacles and make meaningful impacts on patients’ lives.
- • In this role, the individual will develop leadership expertise in statistical programming standards, drive process improvements across therapeutic areas, deepen knowledge of global regulatory requirements (ICH/FDA/EMEA), and gain strategic influence in shaping data standards and submission practices while mentoring teams and collaborating cross-functionally with biostatistics, data management, and clinical teams.
🎯 Requirements
- • BA/BS degree and 12+ years of relevant work experience in data management and analysis within the pharmaceutical or biotechnology industry
- • 12+ years of SAS Base programming experience, including 7+ years using SAS STAT, GRAPH, and MACRO
- • 12+ years of clinical trial experience and 10+ years of clinical database experience
- • Extensive knowledge of the drug development process, CDISC standards (SDTM/ADaM), and submission requirements aligned with ICH, FDA, EMEA, and ROW guidelines
- • Strong management skills with proven ability to lead and collaborate across functions, manage multiple competing priorities, and pay high attention to detail
- • Familiarity with UNIX and experience with R is a plus
🏖️ Benefits
- • Medical, Dental, Vision, and Life insurance coverage
- • Fitness and Wellness programs including fitness reimbursement
- • Minimum of 15 days paid vacation plus end-of-year shutdown (Dec 26–Dec 31), up to 12 company-paid holidays, and 3 paid days for Personal Significance
- • 80 hours of sick time per calendar year
- • Paid Maternity and Parental Leave benefits
- • 401(k) program with company-matched contributions
- • Employee Stock Purchase Plan
- • Tuition reimbursement of up to $10,000 per calendar year
- • Participation in Employee Resource Groups
Skills & Technologies
About Biogen, Inc.
Biogen is an American biotechnology company that develops and manufactures therapies for neurological and neurodegenerative diseases. Founded in 1978, the company focuses on treatments for conditions such as multiple sclerosis, Alzheimer’s disease, spinal muscular atrophy, and amyotrophic lateral sclerosis (ALS). It also produces biosimilar drugs for immune and inflammatory diseases. Biogen operates globally with research, development, and manufacturing facilities supporting its mission to improve outcomes for patients with serious neurological disorders.
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