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Avenzo Therapeutics

Director, Pharmacometrics

Avenzo Therapeutics

. Lead development and execution of pharmacometrics strategies supporting oncology programs .

Posted 10/7/2026full-timeSan Diego • California • United StatesLead💰 $234,000 - $250,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in pharmacometrics and clinical pharmacology, with a strong focus on population PK/PD modeling, regulatory submissions, and strategic leadership in oncology drug development. Proficient in managing cross-functional teams and delivering complex analyses to support dosing strategies and regulatory decision-making.

Highest-signal resume keywords
PhD In PharmacometricsPopulation PK/PD ModelingNONMEM ExpertiseOncology Drug DevelopmentRegulatory Submissions

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Pharmacometric ModelingExposure-Response AnalysisClinical Pharmacology PlansDosing StrategiesStatistical Analysis
Soft Skills
Excellent CommunicationInterpersonal SkillsAnalytical AbilitiesProblem-Solving SkillsStrategic Mindset
Tools & Technologies
NONMEMMonolixRModeling EnvironmentsSimulation Tools
Industry Keywords
Pharmaceutical SciencesBiostatisticsIND FilingsNDA FilingsMAA Filings

About the role

Key responsibilities & impact
  • Lead development and execution of pharmacometrics strategies supporting oncology programs
  • Apply population PK, PK/PD, exposure-response modeling, and simulation analyses to guide dose optimization, study design, and regulatory decision-making
  • Provide strategic leadership and subject matter expertise in pharmacometrics and clinical pharmacology
  • Lead pharmacometric activities on cross-functional program teams with Clinical Development, Biometrics, Regulatory Affairs, and internal and external experts
  • Develop analyses supporting dosing recommendations for special populations, dose modifications, drug–drug interactions, organ impairment, and other factors
  • Resolve complex scientific and technical challenges affecting multiple programs
  • Analyze and interpret clinical and translational PK/PD data and oversee pharmacometric modeling
  • Develop clinical pharmacology plans and dosing strategies from first-in-human through late-stage clinical development
  • Author and review clinical pharmacology content for protocols, clinical study reports, regulatory submissions, briefing documents, and health authority interactions
  • Represent Clinical Pharmacology and Pharmacometrics in regulatory agency meetings and responses
  • Oversee pharmacometric platforms, modeling environments, reporting workflows, and external vendors
  • Manage pharmacometrics activities, budgets, timelines, and deliverables
  • Influence development strategy through quantitative analyses and scientific recommendations
  • Report to the VP, Clinical Pharmacology

Requirements

What you’ll need
  • PhD degree in pharmacometrics, biological/pharmaceutical sciences, bioengineering, biostatistics, engineering, data science, or a related discipline, with 8+ years of progressive pharmacometrics experience in the life sciences industry, or equivalent combination of academic and industry experience
  • Expertise in population PK/PD, exposure-response, and model-informed drug development approaches
  • Extensive hands-on experience with NONMEM, Monolix, R, and other industry-standard modeling and simulation tools
  • Deep understanding of clinical pharmacology and pharmacometric requirements for IND, NDA, MAA, and NDS filings
  • Experience leading and authoring modeling and simulation plans and directing pharmacometric analyses across Phase I–IV clinical development programs
  • Strong knowledge of oncology drug development, clinical pharmacology principles, and regulatory guidelines
  • Ability to manage multiple priorities, projects, and deliverables through influence, matrix leadership, and stakeholder engagement
  • Excellent communication and interpersonal skills
  • Strong analytical and problem-solving abilities with a strategic mindset
  • Willingness to travel periodically/regularly, including up to 15% of work time, potentially overnight
  • Remote employees must travel to and work from the company headquarters in San Diego from time to time
  • San Diego-based employees must work on-site Monday through Thursday

Benefits

Comp & perks
  • Medical, dental, vision, and basic life and AD&D insurance
  • Short-term and long-term disability insurance
  • Flexible spending accounts
  • Health savings accounts
  • Voluntary life, AD&D accident, and critical illness insurance programs
  • 401(k) plan
  • 10 hours of paid vacation time accrued every month
  • 1 hour of paid sick leave accrued for every 30 hours worked
  • 17 paid holidays each calendar year, including a winter closure
  • Annual discretionary bonus
  • Equity award
  • Remote home office arrangement for remote employees
  • Periodic travel and work from company headquarters for remote employees