Senior Director, Global Medical Affairs – Hematology Lead

🔥 1 minute ago

🇺🇸 United States – Remote

💵 $240.4k - $325.2k / year

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

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Amgen

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1980

🧬 Biotechnology

💊 Pharmaceuticals

🔬 Science

💰 $28.5G Post-IPO Debt on 2022-12

Biotechnology • Pharmaceuticals • Science

Amgen is a global leader in biotechnology, focusing on the development and commercialization of innovative medicines made from living cells. The company aims to treat serious illnesses, often targeting diseases with limited therapeutic options. Amgen emphasizes scientific innovation and is committed to ethical research, patient safety, and environmental sustainability. It actively engages in clinical trials and is known for its contributions to the fields of cancer treatment and obesity management among others.

📋 Description

• Join Amgen’s Mission of Serving Patients • Accountability for the development and execution of the global medical affairs strategy across the Hematology portfolio, including marketed products, lifecycle opportunities, and pipeline assets. • Lead, coach, and develop a high-performing global medical hematology team, fostering talent development, succession planning, and organizational effectiveness. • Lead the cross-functional and cross-regional development and execution of the global medical affairs strategy for the assigned asset through the Global Medical Affairs Team. • Serve as the senior Medical Affairs leader for hematology representative on relevant global strategic, governance, and cross-functional teams. • Support development and delivery of the clinical development plan, integrated evidence generation plan, and lifecycle strategy for the assigned asset. • Provide medical and scientific insights to support development of the Target Product Profile and asset strategy. • Capture clinical, scientific, patient, payer, and health system insights across key markets and translate them into concrete strategies and medical plans. • Coordinate with regions to develop and lead external stakeholder management plan, communication strategy, scientific platform, publication plan, and evidence generation plan. • Develop robust external stakeholder engagement and insight-gathering approaches to strengthen understanding of unmet need and maximize the medical value of the asset. • Facilitate scientific engagement with a broad range of external stakeholders, including opinion leaders, professional organizations, advocacy groups, payers, regulators, and other healthcare decision makers. • Provide strategic direction for study design and execution for medical affairs studies and other global evidence-generation activities. • Manage resource and budget allocation necessary to deliver on medical strategies. • Cultivate collaboration and coordination across medical functions, regions, and cross-functional partners. • Ensure all medical activities are conducted in full compliance with applicable laws, regulations, guidelines, and Amgen policies and procedures.

🎯 Requirements

• Doctorate degree and 5 years of medical affairs or clinical development experience in the relevant therapeutic area OR Master’s degree and 8 years of medical affairs or clinical development experience in the relevant therapeutic area OR Bachelor’s degree and 10 years of medical affairs or clinical development experience in the relevant therapeutic area • MD/DO degree from an accredited medical school, PhD, or PharmD. MD plus accredited fellowship or equivalent advanced training in a relevant specialty. • Board certified or board eligible, where applicable. • 5+ years of clinical research and/or medical affairs experience in a leadership role. • Minimum of 5 years of Medical Affairs experience in the biopharmaceutical industry, including biotechnology, pharmaceutical, or CRO experience. • Demonstrated expertise in malignant hematology, including leukemia, lymphoma, myeloma, or related disorders, with a strong understanding of evolving treatment paradigms and competitive landscapes. • Experience building and executing Integrated Evidence Generation Plans. • Demonstrated ability to lead through influence in a matrixed, cross-functional, and cross-regional environment. • Ability to establish effective interactions and engagements with external stakeholders, including opinion leaders, advocacy groups, patients, payers, vendors, professional organizations, and other healthcare decision makers. • Familiarity with global regulatory organizations, guidelines, and practices. • Knowledge of Good Clinical Practices, global regulations, and applicable medical affairs guidelines. • Knowledge of pharmaceutical product development, product lifecycle, and commercialization processes, including clinical operations, commercial, regulatory, safety, access, and medical affairs. • Strong understanding of healthcare systems around the world, including the U.S., Europe, and Asia. • History of solving complex problems while exhibiting sound scientific and medical judgment and a balanced, realistic understanding of issues. • Track record of success working with matrixed cross-functional teams. • Excellent communication, collaboration, strategic planning, and executive presence. • Ability to synthesize complex scientific, clinical, and business information into clear medical strategies and actionable plans.

🏖️ Benefits

• A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions • Group medical, dental and vision coverage • Life and disability insurance • Flexible spending accounts • A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan • Stock-based long-term incentives • Award-winning time-off plans • Flexible work models where possible