Associate Director, In-Vivo Pharmacology
Core
Provide scientific and operational leadership for in-vivo pharmacology strategy in oncology radiopharmaceutical therapeutics (RPT) programs from discovery through IND-enabling development.
Role type
Senior IC Associate Director, In-Vivo Pharmacology
Builds
Preclinical oncology programs advancing toward IND for radiopharmaceutical therapies
Domain
Oncology / Radiopharmaceutical Therapeutics / Preclinical Pharmacology
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
In-vivo oncology pharmacology, Xenograft efficacy studies, Study design and execution, Model selection (CDX/PDX), Dose and schedule rationale, Regulatory compliance (IACUC/AALAC), Cross-functional team leadership, Data interpretation
Preferred skills
Radiopharmaceuticals and radioligand therapies, Dosimetry and radiation biology, AI and computational tools for data analysis, Biodistribution strategy
Technologies
Lu-177, Ac-225, CDX models, PDX models
Responsibilities
Lead in-vivo pharmacology strategy for oncology RPT programs; Provide feedback on model selection, dose rationale, and endpoint definition; Ensure consistency and rigor across in-vivo studies; Own efficacy and biodistribution strategy; Partner with dosimetry, physics, imaging, and radiochemistry teams; Review in-vivo pharmacology sections for regulatory submissions; Escalate animal care and facility issues.
Seniority
Senior, hands-on IC with functional leadership