Senior Director Evidence Delivery

About This Role

The Senior Director, Evidence Delivery leads a global organization responsible for transforming clinical data into high-quality, actionable evidence across the clinical development portfolio. This role drives the strategy, innovation, and operational excellence behind submission-ready datasets, analyses, and visualizations that support regulatory, market access, and publication needs. The Senior Director champions modernization through open-source programming, advanced analytics, automation, and AI/ML. Reporting within SPDDS and QSDO, this leader ensures regulatory compliance, inspection readiness, and continuous improvement while building a future-ready evidence delivery organization.

What You'll Do

• Define and execute the global Evidence Delivery strategy aligned with clinical development and regulatory objectives
• Lead delivery of high-quality, submission-ready datasets, analyses, and visualizations
• Drive adoption of open-source programming platforms such as R and Python
• Champion AI/ML, automation, and advanced analytics to improve efficiency and scalability
• Establish reproducibility, transparency, and traceability frameworks for evidence generation
• Ensure compliance with SOPs, GCP, CDISC standards, and regulatory requirements
• Lead modernization initiatives including cloud computing and workflow automation
• Partner cross-functionally with Statistics, CDM, Regulatory, Safety, Digital, and Market Access teams
• Build, mentor, and retain a high-performing global evidence delivery organization
• Represent Evidence Delivery in audits, inspections, and external industry forums

Who You Are

You are a visionary evidence and analytics leader who thrives in regulated environments and complex global organizations. You combine deep technical expertise with strategic thinking, innovation, and people leadership to deliver high-impact clinical evidence.

Required Skills

• Advanced degree in Statistics, Data Science, Computer Science, or related field
• 15+ years experience in biotech, pharma, CRO, or clinical development environments
• Senior leadership experience in evidence generation or statistical programming
• Deep expertise in SAS and strong knowledge of CDISC standards
• Strong understanding of clinical trial processes and regulatory requirements
• Proven success leading teams in regulated environments
• Experience implementing automation and advanced analytics solutions
• Exceptional stakeholder engagement and communication skills

Preferred Skills

• Experience applying AI/ML in clinical evidence workflows
• Management of external service providers and strategic technology partners

Job Level: Management

Additional Information

The base compensation range for this role is: $254,000.00-$349,000.00

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?

We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.

At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.

All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

Client-provided location(s): Cambridge, MA

Job ID: Biogen-REQ22474

Employment Type: FULL_TIME

Posted: 2026-02-05T00:04:20