Director, Global Medical Affairs – Hematology

This is a fully remote position, open to applicants in United States.

📋 Description

• Implement the designated elements of the integrated global medical strategy for zanubrutinib.

• Convert global priorities into actionable workstreams in collaboration with regional medical teams.

• Monitor execution progress, identify risks and dependencies; escalate challenges and suggest mitigation strategies.

• Facilitate scientific discussions with key opinion leaders, academic institutions, cooperative groups, and professional societies.

• Organize global and/or regional advisory boards, encompassing objectives, agendas, materials, insight capture, and post-meeting outputs.

• Gather, synthesize, and disseminate actionable insights from external engagements.

• Aid in the execution of the Integrated Evidence Plan and conduct evidence gap assessments.

• Assist with concept and protocol evaluations.

• Collaborate with CROs, vendors, and investigators to ensure that study execution aligns with timelines, quality, and compliance standards.

• Implement scientific strategies and deliverables for hematology congresses and peer-reviewed publications.

• Support congress planning, data review sessions, medical booth/medical affairs station assistance, scientific narrative alignment, and internal readiness.

• Guarantee the accuracy, balance, and consistency of scientific messaging.

• Work alongside Clinical Development, Regulatory, Safety, Market Access/HEOR, and Commercial teams while ensuring medical-commercial separation.

• Provide support to regional and affiliate medical teams with coordinated content, scientific updates, and execution toolkits.

• Oversee assigned medical activities and vendor budgets.

• Collaborate with agencies and vendors to ensure timely delivery of high-quality outputs.

⛳️ Requirements

• A minimum of 5 years of progressive experience in medical affairs, clinical development, or similar fields.

• Proven track record in executing global or multi-regional medical initiatives.

• Preferred experience in hematology throughout the product lifecycle, including launch and lifecycle support, evidence generation, and scientific communications.

• Capacity to operate effectively in a fast-paced, matrixed global organization.

• Proficient in coordinating multiple workstreams with a strong focus on quality and timelines.

• Strong scientific aptitude and the ability to interpret and communicate clinical data clearly and equitably.

• Demonstrated operational excellence, project management discipline, and prioritization abilities.

• Familiarity with medical governance, compliance, and quality standards pertinent to Medical Affairs activities.

• Exceptional cross-functional collaboration abilities and capacity to influence within a matrix without direct authority.

• High standards of integrity, accountability, and a patient-centered approach.

• Willingness to travel for work up to 25% domestically and internationally; occasional overtime and weekend travel may be required.

🏝️ Benefits

• Eligibility for an annual bonus plan for non-commercial positions.

• Opportunity to acquire shares of BeOne Medicines Ltd. stock through discretionary equity awards.

• Optional participation in the Employee Stock Purchase Plan.

• Comprehensive medical insurance.

• Dental insurance coverage.

• Vision insurance benefits.

• 401(k) retirement plan.

• Flexible Spending Account (FSA) and Health Savings Account (HSA).

• Life insurance provision.

• Paid Time Off (PTO).

• Wellness benefits offered.