Jobs
Compensation
$183,000 - $229,000
Benefits & Perks
•Healthcare
•Dental
•Vision
•Life Insurance
•Gym
•Disability Insurance
•Parental Leave
•401(k)
•Equity
•Learning Budget
•Healthcare
•Gym
•Parental Leave
•401k
•Equity
•Learning
Required Skills
Evidence Generation
Study design
HEOR
Regulatory knowledge
Project management
Communication
Immunology
Rheumatology
Dermatology
Associate Director, Evidence Generation, Global Medical Lupus
About This Role
Biogen is seeking a dynamic and experienced associate medical director to lead and support evidence generation activities for our Lupus clinical late-stage development programs. Through development, support and execution of a cross-functionally accepted Evidence Generation plan, the Associate Medical Director, Evidence Generation will lead the implementation of a cross-portfolio evidence generation plan and successfully deliver the plan using a balance between therapeutic knowledge, technical expertise, project and communication skills, leveraging and prioritizing internal and external resources as required. This individual contributor role supports a late-stage development program in SLE and CLE and reports to the Global Medical Lead Lupus.
What You’ll Do
As a leader in Evidence Generation, you will play a critical role in shaping and executing scientifically rigorous, impactful research initiatives that enhance our clinical data package and support the broader medical and commercialization strategy. You will:
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Lead or coordinate the design and execution of high-quality evidence generation initiatives, including Phase 3b and IV trials, real-world evidence (RWE) studies, and payer/managed care collaborations.
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Align cross-functional teams (Medical, HEOR, Clin Dev, Epi, Commercial) to ensure evidence strategies support key objectives and inform stakeholders such as HCPs, patients, PAGs, and payers.
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Ensure study compliance with internal SOPs, global regulations, and ethical standards throughout all research activities.
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Track and communicate progress, proactively managing risks, timelines, and mitigation plans to maintain transparency and accountability.
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Engage effectively across audiences, adapting communication to convey complex scientific concepts with clarity and credibility.
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Identify and pursue opportunities for innovation and collaboration, applying a proactive, solution-oriented approach to challenges and learning from outcomes.
Who You Are
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Strong-Proficient in Evidence Generation, phase 4 study design, collaborative research projects and HEOR disciplines such as e.g. comparative effectiveness, the ability to manage multiple studies and present them to stakeholders both within and outside Biogen.
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MD, PhD, PharmD, or comparable advanced degree in a scientific/clinical discipline
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Minimum 5 years’ experience in the healthcare/pharmaceutical sector with 3+ years’ experience in Evidence Generation Roles, including Real World Evidence (RWE)
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High degree of knowledge of global healthcare landscape, public health and industry trends, and regulatory and payer environment to accurately identify key issues and develop evidence generation strategies and plans to strengthen clinical data package
Required Skills
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Clinical experience and subject matter expertise in Immunology, Rheumatology and/or Dermatology
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Experience with medical launch as well as products at different stages of the lifecycle
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Previous collaboration experience with CRO preferred
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Strong working knowledge of global regulations as relevant to Medical Affairs
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Demonstrated ability to effectively lead and collaborate with regional and/or affiliate medical and cross-functional teams to ensure all activities are executed in alignment with global medical strategy and ensuring the insights and needs from them are known and properly addressed
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Ability to manage projects and take initiative to solve complex and challenging problems
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Excellent written and oral communication skills to include presentations
Job Level: Management
Additional Information:
The base compensation range for this role is: $183,000.00-$229,000.00
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