Associate Director, Quantitative Clinical Pharmacology (qcp) Lead

Takeda

Boston, MA, US
Base: $154,400.00 - $242,550.00; bonus/equity: sho...
Hybrid
Quantitative clinical pharmacology expertise
Model-informed drug development midd
Pk pd and pharmacometric analysis
The role involves providing scientific and strategic leadership as a Global or Regional Clinical Pharmacology Lead for multiple projects within the Data and Quantitative Sciences group

Job Summary

  • The role involves providing scientific and strategic leadership as a Global or Regional Clinical Pharmacology Lead for multiple projects within the Data and Quantitative Sciences group.
  • Candidates will be responsible for integrating pharmacokinetic, pharmacodynamic, efficacy, and safety data to optimize dosing strategies across the entire drug development continuum.
  • Takeda offers a competitive base salary range of $154,400.00 to $242,550.00 along with comprehensive benefits including medical insurance, 401(k) matching, and up to 120 hours of paid vacation.

Matching Summary

The role involves providing scientific and strategic leadership as a Global or Regional Clinical Pharmacology Lead for multiple projects within the Data and Quantitative Sciences group.

Salary

Base: $154,400.00 - $242,550.00; Bonus/Equity: Short-term and/or long-term incentives eligible; Benefits: Medical, dental, vision, 401(k) match, disability, life insurance, tuition reimbursement, 120 hours vacation

Skills & Requirements

Must-have

  • Quantitative Clinical Pharmacology expertise
  • Model-Informed Drug Development MIDD
  • PK PD and pharmacometric analysis
  • Regulatory submission leadership
  • Dosage selection and decision making

Nice-to-have

  • Experience with real-world data streams
  • Knowledge of AI and automation tools
  • Cross-functional collaboration skills
  • Scientific publication record
  • Mentoring junior staff capabilities

Key Requirements

  • Pharm D. or PhD degree required
  • 5+ years experience in quantitative field
  • 8+ years experience for MS degree holders
  • Advanced knowledge of regulatory guidance ICH FDA EMA
  • Expertise in cross-functional interfaces with pharmacometrics and statistics

Work Rights

Not specified

Tailored Resume

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