Associate Analyst, Statistical Programming

Responsibilities

• Support coordination, delivery, and review of statistical programming outputs across assigned studies
• Develop CDISC ADaM analysis datasets and specifications; identify and flag data quality issues
• Contribute to end-to-end programming from CRF data collection through regulatory submission
• Support preparation of submission deliverables (define.xml, XPTs, reviewer documentation)
• Collaborate with Biostatistics, Data Management, and Data Standards to ensure consistency and compliance
• Assist with process improvement initiatives and departmental efficiency efforts

Requirements

• Detail-oriented with ability to manage multiple priorities
• Collaborative and comfortable working cross-functionally
• Able to communicate progress, risks, and issues clearly
• Interested in applying statistical programming standards in a clinical environment
• Required skills
• Bachelor's degree in Statistics, Mathematics, or related field
• 0-2 years of SAS programming experience (Base, STAT, GRAPH, MACRO)
• Exposure to clinical trials, data management, or statistical analysis
• Basic knowledge of CDISC standards and clinical data structures
• Understanding of drug development process and regulatory requirements
• Preferred skills
• Master's or PhD in Statistics, Mathematics, or related field
• Experience with regulatory submissions (e.g., define.xml, SDTM/ADaM datasets)
• Familiarity with R, UNIX, or other statistical programming tools
• Knowledge of ICH/FDA guidelines and submission standards
• Job Level: Professional
• Additional Information
• The base compensation range for this role is: $67,000.00-$87,000.00
• Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.
• Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance.
• In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees' and their families physical, financial, emotional, and social well-being; including, but not limited to:
• Medical, Dental, Vision, & Life insurances
• Fitness & Wellness programs including a fitness reimbursement
• Short- and Long-Term Disability insurance
• A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)
• Up to 12 company paid holidays + 3 paid days off for Personal Significance
• 80 hours of sick time per calendar year
• Paid Maternity and Parental Leave benefit
• 401(k) program participation with company matched contributions
• Employee stock purchase plan
• Tuition reimbursement of up to $10,000 per calendar year
• Employee Resource Groups participation
• Why Biogen?

Additional Information

About this role The Associate Analyst, Statistical Programming supports statistical programming activities across clinical studies, including analysis datasets, tables, listings, figures, and regulatory submission deliverables. The role partners with Biostatistics and Data Management to produce high-quality, submission-ready outputs. This position contributes to study timelines, supports implementation of data standards, and assists in resolving data and programming issues under supervision.

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