← 返回岗位列表美国医疗健康与生命科学fulltime

全球医学事务总监 - 血液学(泽布替尼)

雇主

BeiGene

地点

远程 · Remote · 美国

待遇

$USD 192,100 - USD 252,100 / annual

工作模式

远程

截止日期

1月6日

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岗位摘要

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals.

岗位职责

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description:
The Director, Global Medical Affairs – Hematology, within Global Medical Affairs (GMA) is responsible for executing the global medical plan for zanubrutinib. This role ensures that all medical activities are patient-centered, evidence-driven, scientifically credible, and fully compliant, enabling optimal clinical understanding and use of BeOne Medicines therapies.
The Director manages medical activities throughout the product lifecycle in collaboration with GMA hematology leadership and Regional Medical Affairs. The role supports scientific exchange with external stakeholders and ensures delivery of accurate, balanced, and timely scientific information and materials to healthcare professionals.
Essential Function:
Global Medical PlanExecution
Execute assigned components of the integrated global medical plan for zanubrutinib, ensuring high-quality, on-time delivery of tactics and deliverables.
Translate global priorities into executable workstreams in partnership with regional medical teams (e.g., content packages, training toolkits, congress deliverables).
Track execution progress, risks, and dependencies; proactively escalate issues and propose mitigation plans to GMA leadership.
Scientific Exchange & External Engagement
Support scientific exchange activities with key opinion leaders, academic institutions, cooperative groups, and professional societies in alignment with global medical priorities.
Execute advisory boards (global and/or regional), including objectives, agendas, materials development, insight capture, and post-meeting outputs.
Capture, synthesize, and communicate actionable insights from external interactions to inform ongoing medical execution and cross-functional alignment.
Evidence Generation
Support execution of the Integrated Evidence Plan through delivery of Integrated Evidence Plans initiatives.
Support concept & protocol reviews and evidence gap assessment for assigned therapeutic areas.
Coordinate with internal and external partners (CROs, vendors, investigators) to ensure study conduct aligns with timelines, quality expectations, and compliance requirements.
Scientific Communications & Publications
Execute scientific tactics and deliverables for key hematology congresses (e.g., ASH, EHA, ASCO) and peer-reviewed journals.
Support congress planning execution including data review meetings, medical booth/medical affairs station support, scientific narrative consistency, and internal readiness.
Ensure scientific accuracy, balance, and consistency of messaging across global and regional scientific materials.
Cross-Functional & Regional Collaboration
Collaborate with Clinical Development, Regulatory, Safety, Market Access/HEOR, and Commercial teams while maintaining appropriate medical-commercial separation.
Support regional and affiliate medical teams with aligned content, scientific updates, and execution toolkits; enable consistent global scientific narrative across geographies.
Operations & Vendor Management
Manage assigned budgets for medical activities and vendors; ensure efficient resource utilization and timely purchase order/contract processes in partnership with operations.
Coordinate with agencies and vendors (medical communications, digital, congress logistics) to deliver high-quality outputs on schedule
Minimum Requirements – Education and Experience:
Minimum of 5 years of progressive experience in medical affairs, clinical development, or related roles, with demonstrated execution of global or multi-regional medical activities
Experience in hematology across the product lifecycle, including launch and lifecycle support, evidence generation, and scientific communications preferred.
Demonstrated ability to execute in a fast-paced, matrixed, global organization and coordinate multiple workstreams with strong attention to quality and timelines
Other Experience:
Strong scientific acumen and ability to interpret and communicate clinical data with clarity and balance.
Operational excellence, project management discipline, and prioritization skills.
Knowledge of medical governance, compliance, and quality standards for Medical Affairs activities.
Excellent cross-functional collaboration skills and ability to influence in a matrix without direct authority.
High standards of integrity, accountability, and patient-centered mindset.
Supervisory Responsibilities:
None
Travel:
Work-related travel up to 25% domestic/international.
Overtime and weekend travel may be occasionally required.
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
Fosters Teamwork
Provides and Solicits Honest and Actionable Feedback
Self-Awareness
Acts Inclusively
Demonstrates Initiative
Entrepreneurial Mindset
Continuous Learning
Embraces Change
Results-Oriented
Analytical Thinking/Data Analysis
Financial Excellence
Communicates with Clarity
Salary Range:$192,100.00 - $252,100.00 annuallyBeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact .
Originally posted on Himalayas

申请条件

- 具有科学或商业专业背景,经验丰富
- 高度积极主动,善于协作
- 对抗击癌症有强烈热情和兴趣
- 具备全球医学事务或相关领域经验
- 能够执行全球医学计划并确保高质量按时交付
- 能够将全球优先事项转化为可执行的工作流
- 具备与区域医学团队合作的能力
- 能够跟踪执行进度、风险和依赖关系,并主动上报问题
- 能够支持与关键意见领袖、学术机构、合作团体和专业学会的科学交流活动
- 具备执行顾问委员会的经验,包括目标设定、议程、材料开发、洞察收集和会后输出
- 能够捕获、综合和传达外部互动中的可操作洞察
- 具备血液学领域知识或经验
- 了解产品生命周期管理
- 具备合规意识,确保所有医学活动以患者为中心、循证、科学可信且完全合规
- 能够向医疗专业人士提供准确、平衡和及时的科学信息和材料

雇主简介

BeiGene is a global, science-driven biopharmaceutical company focused on developing innovative medicines for cancer and expanding into immunology and inflammation therapies.

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数据来源:Himalayas

岗位信息来源于公开渠道,版权归原作者所有