Global Clinical Program Lead, HematologyAstraZeneca · US - South San Francisco - CA
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AstraZeneca

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Global Clinical Program Lead, Hematology

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🗓️ Posted 2026-08-28 US - South San Francisco - CA Full-time Hybrid Healthcare Medical
💰 Salary Not shared 📊 Market 20,000 CAD–35,000 CAD/mo

About the Company

We're transforming the future of healthcare by unlocking the power of what science can do for people, society and the planet. For more information, visit www.astrazeneca.com. Community Guidelines: bit.ly/2MgAcio Pharmaceutical Manufacturing Specialties: Pharmaceutical, Biopharmaceutical, Innovation, Research and development, Global business

Responsibilities

  • ● Role: Global Clinical Program Lead, Hematology
  • ● Hybrid Working: Minimum of 3 days per week in the office
  • ● AstraZeneca has a multifaceted environment that cultivates collaboration and innovation. We attract top minds, and we nurture and build talent.
  • ● Within Hematology R&D, we are committed to advancing the science to deliver life-changing medicines to patients most in need. With a combination-focused pipeline that exploits the power of six scientific platforms (Immuno-Oncology, Tumor Drivers and Resistance, DNA Damage Response, Antibody-drug Conjugates, Cell Therapy and Epigenetics) to help address unmet clinical needs in a host of hematological cancers, we are motivated by a dedication to the scientific discovery and collaboration that will one day help eliminate cancer as a cause of death. This unit has responsibility for the value chain from discovery through to late-stage development, enabling rapid acceleration of promising early-stage assets and life-cycle management programs.
  • ● The Hematology Research and Early Development (R&D) team has the accountability for all drug development activities in hematology research from first in man studies, all the way to late-stage trials leading to drug approval by regulatory agencies (Phase 1, 2 and 3 trials). The team strives to deliver compelling preclinical, clinical and translational data packages providing confidence in the dosing strategy, tolerability profile and therapeutic efficacy of our candidate drugs to support investment in late stage clinical development, leading to drug approval.
  • ● In this role the candidate will work with other project leaders, scientific and clinical leaders as well as external experts to coordinated integrated project plans which can be delivered across functional boundaries. The candidate will ensure that diverse views within the team are heard and that a strongly empowered and motivated team is created, and will demonstrate highly visible leadership within the oncology community, both within AZ and externally. The successful candidate will have hematology/oncology clinical drug development experience, demonstrated leadership, and be able to critically navigate the science that underlies these programs. The candidate should be able to effectively communicate across a broad range of audiences and have an ability to clearly articulate project specific strategies as well as the overall oncology strategy.
  • ● Leads clinical development teams responsible for novel Hematology Oncology therapies from preclinical candidate selection through proof of concept leading to Phase 3 investment decisions. The candidate will lead all regulatory submissions. Accountable for the clinical strategy and clinical execution of a portfolio of pre-clinical and clinical stage therapies.
  • ● Accountable for the delivery of project according to quality, time, budgets and resources
  • ● Build strategic and coordinated clinical development plans which are aligned with business objectives and are differentiated from competitor products.
  • ● Accountable for the execution of the integrated product plan to agreed scope, timelines, and budgets
  • ● Leads and communicates the clinical development strategy at governance meetings, accountable for aligning with internal management and for communicating with external collaborators.
  • ● Lead clinical aspects of projects from preclinical Lead Optimization Investment Decision to clinical Proof of Concept (PoC):
  • ● Responsible for all clinical aspects of project strategy including translational, clinical development, patient selection, regulatory, pediatric, and Asian development strategy
  • ● Development of the Target Product Profile, ensuring alignment with disease area strategy and late stage development
  • ● Co-leads the Clinical ProgramTeam (CPT) to effectively run/mitigate/communicate risk, make decisions, and handle conflict and change.
  • ● Responsible for maintaining a high degree of CPT effectiveness through collaboration, influence, and, as necessary, coaching and mentoring of cross-functional team members.
  • ● Ensure that there are robust processes, plans and data to enable Governance Bodies to make investment decisions and prioritize projects across the portfolio.
  • ● Minimum Qualifications:
Credential Requirements for Canada
🔴

MCCQE Part I + II

Medical Council of Canada

Must have to work
Cost: CAD 1,200–2,500 Timeline: 1–2 years
🔴

NNAS Assessment + NCLEX-RN

National Nursing Assessment Service

Must have to work
Cost: CAD 650–1,200 Timeline: 6–12 months
🔴

PEBC Evaluating Exam + Qualifying Exam + Provincial Licence

Pharmacy Examining Board of Canada

Must have to work
Cost: CAD 1,500–3,000 Timeline: 1–2 years
🔴

NDEB Equivalency Process + OSCE

National Dental Examining Board of Canada

Must have to work
Cost: CAD 3,000–5,000 Timeline: 1–3 years