Global Development Leader - Clinical Strategy & Trials

Nurix, Inc.

California, Northern (MO, KY)

Hybrid

USD 300,000 - 420,000

Full time

14 days+
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Job summary

Nurix Therapeutics seeks a strategic and hands-on Vice President / Senior Vice President, Global Development Leader to oversee programs from phase 1 through launch. You will partner with Clinical Operations, Regulatory, Quality, and Commercial teams to drive program strategy and execution while ensuring safety and regulatory compliance.

The role requires MD/PhD-level leadership with 10+ years in clinical trials, strong leadership, and excellent communication in a fast-paced biopharma setting.

Qualifications

  • MD with board certification in hematology/oncology.
  • At least 10 years of clinical trial experience in the pharmaceutical industry.
  • Ph3 trial design and execution experience.
  • Strong leadership and cross-functional collaboration.
  • Excellent communication in a fast-paced environment.

Responsibilities

  • Lead one or more Clinical Development Program teams from phase 1 to launch.
  • Set direction for a portfolio of clinical stage therapies aligned with corporate goals.
  • Develop and communicate program plans with asset teams and program management.
  • Facilitate cross-functional communication and governance.
  • Provide medical oversight for ongoing trials and CROs.
  • Engage investigators and thought leaders to advance trials.
  • Refine processes for design and data reporting of trials.
  • Present data to executives and external medical colleagues.

Skills

Leadership
Cross-functional collaboration
Strategic program leadership
Communication

Education

MD, board certified in hematology/oncology

Job description

Nurix Therapeutics seeks a strategic and hands-on Vice President / Senior Vice President, Global Development Leader to oversee programs from phase 1 through launch. You will partner with Clinical Operations, Regulatory, Quality, and Commercial teams to drive program strategy and execution while ensuring safety and regulatory compliance.

The role requires MD/PhD-level leadership with 10+ years in clinical trials, strong leadership, and excellent communication in a fast-paced biopharma setting.

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