Associate Director, Quantitative Clinical Pharmacology (qcp) Lead

Takeda

Boston, MA, United States
Base: $153,600.00 - $241,340.00; bonus/equity: eli...
Hybrid
Clinical pharmacology leadership
Model-informed drug development (midd)
Pharmacokinetic and pharmacodynamic analysis
Takeda is a global, values-based, R&D-driven biopharmaceutical leader committed to delivering life-transforming treatments guided by commitment to patients, people, and the planet

Job Summary

  • Takeda is a global, values-based, R&D-driven biopharmaceutical leader committed to delivering life-transforming treatments guided by commitment to patients, people, and the planet.
  • The role leads strategic, scientific, and operational aspects of multiple drug development projects with high technical and strategic independence from first in human dosing through life cycle management.
  • U.S. based employees may be eligible for short-term and/or long-term incentives, comprehensive benefits including medical, dental, vision insurance, 401(k) plan with company match, paid volunteer time off, and vacation accrual.

Matching Summary

Takeda is a global, values-based, R&D-driven biopharmaceutical leader committed to delivering life-transforming treatments guided by commitment to patients, people, and the planet.

Salary

Base: $153,600.00 - $241,340.00; Bonus/Equity: Eligible for short-term and/or long-term incentives; Benefits: Medical, dental, vision, 401(k), disability, life insurance, tuition reimbursement, paid time off

Skills & Requirements

Must-have

  • clinical pharmacology leadership
  • Model-Informed Drug Development (MIDD)
  • pharmacokinetic and pharmacodynamic analysis
  • regulatory submission expertise
  • cross-functional collaboration
  • dose selection and decision-making

Nice-to-have

  • mentoring junior staff
  • scientific publications and presentations
  • experience with digital health and outcomes research
  • participation in scientific societies
  • business development due diligence

Key Requirements

  • PharmD or PhD with 5+ years experience
  • MS with 8+ years experience
  • experience in clinical pharmacology/PK-PD
  • knowledge of regulatory guidance (ICH, FDA, EMA)
  • experience in early and late stage clinical studies

Work Rights

Not specified

Tailored Resume

Cover Letter