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Associate Director, Pharmacology

💼 Full-time💰 $177,500–$177,500🗓 2026-09-07

Core

Shape and execute preclinical pharmacology strategy across development programs to advance assets efficiently, defining studies and evidence packages for high-quality program decisions.

Role type

Associate Director, preclinical pharmacology strategy

Builds

Preclinical pharmacology studies and integrated evidence packages for drug development

Domain

Biopharma, preclinical pharmacology, immunology

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

preclinical pharmacology strategy, mechanism of action characterization, in vivo proof of concept design, PK/PD analysis, CRO study management, translational hypothesis generation, regulatory positioning, cross-functional partnership

Preferred skills

immunology expertise, AI-enabled scientific workflows, data analytics, modeling

Technologies

AI-enabled tools, modeling, data analytics, organizational tracking systems

Responsibilities

Design and oversee pharmacology studies to characterize mechanism of action, target biology, and dose-response; Develop integrated pharmacology plans covering efficacy, biomarkers, and therapeutic index; Partner with DMPK, Toxicology, and Regulatory teams to integrate pharmacology into development strategy; Manage CRO-executed studies including protocol review, vendor oversight, and data quality; Apply first-principles reasoning to evaluate biological rationale and design focused studies

Seniority

Senior, hands-on IC with strategic oversight

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