Global Development Leader - Clinical Strategy & Trials

Nurix Therapeutics; Brisbane (CA); On-site; USD 350,000 - 520,000; Full time

Job summary

Nurix Therapeutics is seeking a Vice President / Senior Vice President, Global Development Leader to provide strategic medical leadership across clinical programs from Phase 1 through approval and launch. The role requires leadership across Clinical Development, Regulatory, and Quality functions, with a focus on safety and regulatory compliance.

The ideal candidate has MD credentials with hematology/oncology board certification and at least 10 years of Ph3 experience in pharma, demonstrating

Qualifications

• MD, board certified preferably in hematology/oncology.
• Requires at least 10 years’ clinical trial experience in the pharmaceutical industry with involvement in Ph3 design or execution.
• Excellent communicator with proven leadership and cross-functional interaction skills.

Responsibilities

• Lead one or more Program teams spanning Clinical Development, Regulatory, Quality, and other functions from Phase 1 through approval and launch; own BTK Program GDT accountability.
• Set direction and execute portfolio strategy aligned with corporate goals.
• Develop and communicate program plans and development plans with asset teams and program management.
• Drive cross-functional alignment and mitigate emerging challenges.
• Provide medical oversight for ongoing trials and CRO activities; ensure safety and regulatory compliance.
• Interact with investigators and thought leaders to support trials and data interpretation.
• Oversee training and medical input for the clinical team and regulatory discussions.

Skills

MD

Leadership

Cross-functional collaboration

Communication

Strategic thinking

Education

MD, board certified in hematology/oncology

Job description

Nurix Therapeutics is seeking a Vice President / Senior Vice President, Global Development Leader to provide strategic medical leadership across clinical programs from Phase 1 through approval and launch. The role requires leadership across Clinical Development, Regulatory, and Quality functions, with a focus on safety and regulatory compliance.

The ideal candidate has MD credentials with hematology/oncology board certification and at least 10 years of Ph3 experience in pharma, demonstrating