Associate Director, In‑Vivo Oncology Pharmacology

Bristol-Myers Squibb Co; San Diego (CA); On-site; USD 191,000 - 231,000; Full time

Benefits offered by this job

Comprehensive benefit plans

Flexible Time Off

Paid holidays

Volunteer days

Life insurance

Disability insurance

Job summary

RayzeBio is seeking an Associate Director of In‑Vivo Pharmacology to lead oncology radiopharmaceutical programs from discovery through IND‑enabling development. You will guide study design, data interpretation, and translational relevance while ensuring regulatory alignment and animal welfare compliance.

The role requires a PhD with 8+ years in industry, a track record in xenograft efficacy, and the ability to lead cross‑functional teams.

Qualifications

• Ph.D. required with 8+ years of industry experience.
• Strong track record in in‑vivo oncology pharmacology and preclinical programs.
• Experience leading cross‑functional teams and pragmatic decision making.
• Knowledge of IACUC processes and animal welfare regulations.
• Experience applying AI/computational tools to data analysis is desirable.

Responsibilities

• Lead the in‑vivo pharmacology strategy for oncology radiopharmaceutical programs.
• Provide scientific feedback on model selection, dose rationale, and endpoints.
• Support mouse strains, tumor models, and fractionation schemes for RPT isotopes.
• Ensure rigor and alignment of in‑vivo studies across programs from discovery to IND‑enabling development.
• Oversee efficacy and biodistribution strategies and cross‑team collaboration.
• Review in‑vivo pharmacology sections of reports and regulatory submissions.

Skills

In‑Vivo pharmacology

Cross-functional leadership

Decision making

Regulatory compliance

AI/data analysis

Education

Ph.D. in Pharmacology, Cancer Biology, Toxicology

Tools

AI tools

Dosimetry collaboration

Job description

RayzeBio is seeking an Associate Director of In‑Vivo Pharmacology to lead oncology radiopharmaceutical programs from discovery through IND‑enabling development. You will guide study design, data interpretation, and translational relevance while ensuring regulatory alignment and animal welfare compliance.

The role requires a PhD with 8+ years in industry, a track record in xenograft efficacy, and the ability to lead cross‑functional teams.