채용
Compensation
$254,000 - $349,000
Benefits & Perks
•Healthcare
•401(k)
•Equity
•Parental Leave
•Learning Budget
•Gym
•Healthcare
•401k
•Equity
•Parental Leave
•Learning
•Gym
Required Skills
SAS
Statistical Programming
CDISC Standards
Clinical Trial Processes
Team Leadership
Regulatory Compliance
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.
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About Biogen

Biogen
PublicSpecializing in the treatment of neurological diseases.
5,001-10,000
Employees
Cambridge
Headquarters
Reviews
4.1
47 reviews
Work Life Balance
3.6
Compensation
4.7
Culture
4.1
Career
4.4
Management
3.8
84%
Recommend to a Friend
Pros
Opportunities for continuous learning and growth
Strong engineering culture with focus on code quality
Cutting-edge technology stack and interesting technical challenges
Cons
Organizational changes and restructuring can be disruptive
Fast-paced environment with tight deadlines
Work-life balance can be challenging during product launches
Salary Ranges
541 data points
Mid/L4
Senior/L5
Mid/L4 · SR Analyst, R&D Business Ops
1 reports
$131,388
total / year
Base
$114,250
Stock
-
Bonus
-
$131,388
$131,388
Interview Experience
47 interviews
Difficulty
3.5
/ 5
Duration
14-28 weeks
Offer Rate
36%
Experience
Positive 65%
Neutral 25%
Negative 10%
Interview Process
1
Phone Screen
2
Technical Interview
3
System Design
4
Behavioral
5
Team Fit
Common Questions
Tell me about a challenging project
System design question
Coding problem
Why this company
News & Buzz
FDA grants breakthrough therapy designation to Biogen’s litifilimab - Investing.com
Source: Investing.com
News
·
5w ago
Biogen’s Litifilimab Receives FDA Breakthrough Therapy Designation for Cutaneous Lupus Erythematosus, a Disease With No Targeted Treatment Options - Biogen
Source: Biogen
News
·
5w ago
FDA Accepts LEQEMBI® IQLIK™ (lecanemab-irmb) Supplemental Biologics License Application as a Subcutaneous Starting Dose for the Treatment of Early Alzheimer’s Disease under Priority Review - Biogen
Source: Biogen
News
·
5w ago
Biogen’s Alisha Alaimo On The Company’s Next Big Commercial Build - Citeline News & Insights
Source: Citeline News & Insights
News
·
6w ago