Medical Lead - Acute Lymphoblastic Leukemia (ALL)

AstraZeneca•Gaithersburg, MD
•$193,282 - $289,922•Hybrid

About The Position

The Medical Lead, Acute Lymphoblastic Leukemia (ALL) will help shape and deliver the US Medical Affairs strategy for a priority hematology oncology indication. This highly visible role leads the Core Medical Team, develops and executes the integrated medical plan, and applies scientific, clinical, customer, and multi-channel insights to inform evidence generation, product development, and launch readiness. The role collaborates across Medical, Clinical Development, Patient Safety, Commercial, Market Access, and Field Medical teams to advance science-driven strategies with meaningful impact for patients and the CLL community. The Medical Lead manages investigator-initiated studies that complement AstraZeneca’s clinical development plan, leads real-world evidence strategy from concept through execution and communication, and creates the US publication plan for generated evidence. The role also provides medical review and input for key materials, engages strategic external partners, contributes to safety discussions, and supports scientific exchange with field medical and key account teams. This is a hybrid role based in Gaithersburg, Maryland, with an average minimum of three days per week in the office and travel nationally and internationally, as appropriate, up to approximately 30% of the time.

Requirements

  • Doctorate in Medicine (M.D. or D.O.), PhD, or PharmD degree, plus proven experience.
  • At least 5 years of related work experience in industry, a clinical institution, or a research institution; preferably in onco-hematology, solid tumors, or related areas.
  • 1–3 years in a headquarters Medical Affairs role.
  • Expert technical depth in Hematology/Oncology.
  • Thorough understanding of drug development and pharmaceutical market support, and in-depth knowledge of Hematology/Oncology, including clinical evidence and real-world patient management.
  • Strong leadership with a proven track record of change and impact.
  • Strong business acumen and experience with financial management.
  • Ability to work productively with commercial and scientific/medical colleagues, including Clinical Development teams, and to engage and influence senior stakeholders in cross-functional teams.
  • Ability to travel nationally and internationally, as appropriate, up to approximately 30% of the time.
  • Excellent written and oral communication, interpersonal, negotiation, and presentation skills.

Nice To Haves

  • Active license as an M.D., D.O., PhD, or PharmD professional.
  • Additional training such as an M.P.H., M.B.A., or other advanced degree.
  • Product launch experience and knowledge of FDA requirements.
  • Experience working in the US market.
  • Experience supporting brands or disease areas in-country, regional, or global organizations.
  • Experience with clinical management of leukemia, chronic and/or acute.
  • Experience in evidence generation planning and clinical trial design.
  • Experience in a Medical Affairs strategy-setting role and navigating sophisticated business challenges.
  • Experience developing and maintaining a network that includes third-party experts.
  • Background in practicing medicine or clinical research, and familiarity with biostatistics, epidemiology, and health outcomes.
  • Knowledge of relevant professional societies and scientific medical experts.
  • People leadership experience, including demonstrated coaching and mentoring.

Responsibilities

  • Lead the Core Medical Team and develop and execute the integrated medical plan for the assigned indication.
  • Use scientific, clinical, customer, and multi-channel insights to inform evidence generation, product development, and launch readiness.
  • Collaborate with Medical, Clinical Development, Patient Safety, Commercial, Market Access, and Field Medical teams.
  • Manage investigator-initiated studies that complement the AstraZeneca clinical development plan.
  • Lead the real-world evidence strategy for the assigned indication or asset from concept through execution and communication.
  • Create the US publication plan for generated evidence.
  • Provide medical review and input for key materials.
  • Engage strategic external partners.
  • Contribute to safety discussions.
  • Support scientific exchange with field medical and key account teams.

Benefits

  • Short-term incentive bonus eligibility.
  • Equity-based award eligibility for salaried roles.
  • Qualified retirement programs.
  • Paid time off, including vacation, holiday, and leaves.
  • Health coverage.
  • Dental coverage.
  • Vision coverage.
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