Prostate Cancer Clinical Development Leader

Regulatory Jobs

United States

Remote

USD 307,000 - 372,000

Full time

6 days ago

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Benefits offered by this job

Flexible Time Off

11 paid holidays

Medical insurance

Stock opportunities

Job summary

RayzeBio, a Bristol Myers Squibb affiliate, seeks a Senior Director of Clinical Development to lead prostate cancer programs. You will direct Phase 1–3 trials, guide regulatory interactions, and build strong cross-functional teams in a highly regulated, fast-moving environment.

Ideal candidates bring 10+ years in oncology development, MD/PhD/PharmD, and experience with NDA/MAA processes. Willingness to travel ~30% and contribute to strategic planning is essential.

Qualifications

MD/PhD/PharmD with oncology focus and 10+ years in oncology clinical development.
Experience in NDA/MAA submissions and global health authority interactions.
Proven ability to lead cross-functional teams and manage stakeholders.
Experience with radiopharmaceuticals or radioligand therapies preferred.

Responsibilities

Provide clinical direction for Phase 1–3 trials in prostate cancer.
Lead cross-functional study teams and supervise medical directors.
Oversee regulatory interactions and briefing documents.
Collaborate with research, translational medicine, and BD teams.
Develop and execute clinical development strategies and plans.
Travel approximately 30% as needed.

Skills

Clinical Development

Regulatory Strategy

Leadership

Cross-functional Leadership

ICH/GCP Knowledge

Communication Skills

Oncology Expertise

Education

MD/PhD/PharmD

Job description

Ideal candidates bring 10+ years in oncology development, MD/PhD/PharmD, and experience with NDA/MAA processes. Willingness to travel ~30% and contribute to strategic planning is essential.

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