Lead, Late-Stage Oncology Clinical Development

Zai Lab (US) LLC

South San Francisco (CA)

On-site

USD 292,000 - 409,000

Full time

14 days+

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Job summary

Zai Lab is seeking a Senior Medical Director, Oncology Clinical Development, to lead late-stage oncology programs, including pivotal trials and regulatory submissions. The role requires MD with oncology board certification and at least five years in clinical development, with strong cross-functional collaboration and external representation.

The position is based in our South San Francisco office, with travel up to 30% and a focus on strategy, safety monitoring, and global regulatory engagement.

Qualifications

  • MD with board certification in Oncology, Hematology-Oncology, or a related specialty.
  • Five years of clinical development experience, with a focus on late-stage oncology trials.

Responsibilities

  • Provide medical leadership for the design and execution of late-stage oncology trials, including pivotal studies.
  • Serve as Medical Monitor for Phase III and registration trials, ensuring patient safety and protocol compliance.
  • Contribute expert medical leadership to regulatory submissions and lifecycle planning.
  • Collaborate with regulatory affairs, clinical operations, pharmacovigilance, biostatistics, medical affairs, and commercial teams.
  • Represent Zai Lab in interactions with investigators, key opinion leaders, regulators, and external collaborators.
  • Analyze trial data and real-world evidence to identify trends and support data-driven decisions.
  • Develop strategies for label expansion and long-term product differentiation.
  • Lead regulatory documentation and health authority interactions globally.

Education

MD with board certification in Oncology, Hematology-Oncology, or a related specialty

Job description

Zai Lab is seeking a Senior Medical Director, Oncology Clinical Development, to lead late-stage oncology programs, including pivotal trials and regulatory submissions. The role requires MD with oncology board certification and at least five years in clinical development, with strong cross-functional collaboration and external representation.

The position is based in our South San Francisco office, with travel up to 30% and a focus on strategy, safety monitoring, and global regulatory engagement.

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