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About This Role
The Associate Director, Global Program Management will lead complex, cross-functional programs spanning Medical, Regulatory, Clinical Development, Quality, Supply Chain, and Commercial interfaces. This role is accountable for shaping strategy, driving execution, overseeing governance, improving operational frameworks, and ensuring transparency and alignment across senior leadership.
In this role, you will provide strategic, programmatic, and operational leadership across a portfolio of global R&D or early-stage access-related initiatives.
What You'll Do
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Drive the strategic direction, operating model, and long-term roadmap for a diverse portfolio of global programs.
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Lead complex, multi-asset, multi-region, and cross-functional initiatives across the organization.
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Translate business strategy into actionable program plans, milestones, KPIs, and measurable outcomes.
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Partner with stakeholders across R&D, Medical, Regulatory, Quality, Supply Chain, Finance, Legal, and Commercial functions to ensure alignment and decision-making.
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Develop and maintain integrated program plans, timelines, governance structures, reporting cadences, and critical paths.
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Identify program risks, dependencies, and issues, while implementing mitigation plans and driving operational excellence.
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Lead process improvement and optimization initiatives to enhance efficiency, transparency, and execution.
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Oversee portfolio prioritization, budget forecasting, financial tracking, scenario planning, and resource allocation.
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Lead, mentor, and develop project managers and program professionals while fostering accountability, collaboration, and high performance.
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Prepare and present executive-level updates, dashboards, risk assessments, portfolio insights, and strategic recommendations.
Who You Are
You are an experienced global program leader with a strong background in pharmaceutical, biotech, or healthcare environments, ideally including Managed Access or Expanded Access Programs. You are highly autonomous, able to translate objectives into actionable plans, manage day-to-day execution independently, and drive programs forward with minimal oversight. You are also a strong communicator who knows when to escalate risks, align stakeholders, and provide clear updates to senior leadership.
Required Skills
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8-12+ years of relevant experience in biopharmaceutical, healthcare, or R&D program management.
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Bachelor’s degree required; advanced degree preferred.
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Expertise in global program management within biopharmaceutical, R&D, or healthcare environments.
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Required experience with Charged Managed Access Programs (CMAP) and broader Managed Access or Expanded Access initiatives.
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Strong strategic thinking, decision-making, and problem-solving capabilities.
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Excellent communication, stakeholder management, and executive presentation skills.
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Experience managing external vendors, partners, and cross-functional collaborations.
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Strong organizational, planning, and project management abilities.
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Proven ability to manage multiple priorities, timelines, and stakeholders (including executives) in a global matrixed environment.
Job Level: Management
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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Biogenについて

Biogen
PublicSpecializing in the treatment of neurological diseases.
5,001-10,000
従業員数
Cambridge
本社所在地
$16.2B
企業価値
レビュー
4.1
10件のレビュー
ワークライフバランス
3.8
報酬
4.2
企業文化
4.3
キャリア
3.5
経営陣
4.0
78%
友人に勧める
良い点
Supportive management and team culture
Excellent health benefits and compensation
Flexible working arrangements and remote options
改善点
Heavy workload and long hours during deadlines
High-pressure environment leading to stress and burnout
Limited growth potential in some departments
給与レンジ
545件のデータ
M3
M4
M5
M6
Senior/L5
M3 · Product Manager M3
0件のレポート
$199,467
年収総額
基本給
$79,787
ストック
$99,734
ボーナス
$19,947
$139,627
$259,307
面接体験
47件の面接
難易度
3.5
/ 5
期間
14-28週間
内定率
36%
体験
ポジティブ 65%
普通 25%
ネガティブ 10%
面接プロセス
1
Phone Screen
2
Technical Interview
3
System Design
4
Behavioral
5
Team Fit
よくある質問
Tell me about a challenging project
System design question
Coding problem
Why this company
ニュース&話題
Notable analyst calls this week: Tesla, Qualcomm and Biogen among top picks - Seeking Alpha
Seeking Alpha
News
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3d ago
Spotify, Sandisk, Natera, Biogen, Tesla Trending With Analysts - TipRanks
TipRanks
News
·
3d ago
Biogen Inc. (NASDAQ:BIIB) Given Consensus Recommendation of "Hold" by Brokerages - MarketBeat
MarketBeat
News
·
3d ago
The Late Miocene-Early Pliocene biogenic bloom in oligotrophic waters of the South Atlantic Subtropical Gyre
·
4d ago
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