Senior Clinical Lead, Oncology Solid Tumor Trials

Astellas Pharma

Northbrook (IL)

Hybrid

USD 207,000 - 296,000

Full time

14 days+

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Benefits offered by this job

Medical Insurance
Dental Insurance
Vision Insurance
401(k) match

Job summary

Astellas Pharma, based in Northbrook, Illinois, seeks an experienced clinical development leader to oversee and drive trial strategies in Immuno-Oncology. The role covers both late and early-phase programs, coordinating with global teams to ensure safety, data quality, and regulatory readiness.

You will lead protocol development, site oversight, and cross-functional collaboration with medical affairs, pharmacology, and regulatory to shape trial execution and outcomes.

Qualifications

  • MD or MD/PhD with oncology fellowship completed.
  • 5+ years in pharma or academia in clinical trial design and execution.
  • Proven record designing trials that yield high-quality data.
  • Experience as medical monitor and coordinating trial execution.
  • Excellent English communication and global collaboration skills.

Responsibilities

  • Collaborate with asset teams and lead clinical study teams on trials.
  • Serve as Medical Monitor and ensure patient safety across studies.
  • Plan dose selection, escalation and safety management for programs.
  • Integrate translational inputs into development strategies and trial designs.
  • Develop regulatory documents and ensure alignment with strategy.
  • Present clinical development plans at governance meetings.

Skills

Communication skills
Global teamwork
Clinical trial design
Regulatory knowledge
Bio-pharma industry experience

Education

MD or MD/PhD with oncology fellowship

Job description

Astellas Pharma, based in Northbrook, Illinois, seeks an experienced clinical development leader to oversee and drive trial strategies in Immuno-Oncology. The role covers both late and early-phase programs, coordinating with global teams to ensure safety, data quality, and regulatory readiness.

You will lead protocol development, site oversight, and cross-functional collaboration with medical affairs, pharmacology, and regulatory to shape trial execution and outcomes.

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