Clinical Scientist Associate Director, Late Development Obesity

Amgen

Remote
Base: 183,251.00 usd - 223,386.00 usd; bonus/equit...
Hybrid
Late-phase clinical development
Protocol development
Data review and monitoring
The Clinical Scientist Associate Director supports late-phase clinical development by contributing to protocol development, study start-up, data review and monitoring and analysis activities

Job Summary

  • The Clinical Scientist Associate Director supports late-phase clinical development by contributing to protocol development, study start-up, data review and monitoring and analysis activities.
  • This role focuses on study-level implementation and cross-functional coordination to help ensure high-quality, decision-ready clinical data.
  • Amgen offers a comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts.

Matching Summary

The Clinical Scientist Associate Director supports late-phase clinical development by contributing to protocol development, study start-up, data review and monitoring and analysis activities.

Salary

Base: 183,251.00 USD - 223,386.00 USD; Bonus/Equity: Discretionary annual bonus program, Stock-based long-term incentives; Benefits: Comprehensive employee benefits package, Retirement and Savings Plan, group medical, dental and vision coverage, life and disability insurance, flexible spending accounts

Skills & Requirements

Must-have

  • Late-phase clinical development
  • Protocol development
  • Data review and monitoring
  • Cross-functional coordination
  • Clinical trial process improvements

Nice-to-have

  • Collaborative and innovative culture
  • Passion for challenges
  • Science-based approach
  • Strong communication and presentation skills

Key Requirements

  • Doctorate degree and 3 years of clinical development experience
  • Master’s degree and 5 years of clinical development experience
  • Bachelor’s degree and 7 years of clinical development experience
  • Associate’s degree and 12 years of clinical development experience
  • High school diploma / GED and 14 years of clinical development experience
  • 3 years of pharmaceutical clinical drug development experience
  • Experience supporting early or late-phase drug development
  • Experience supporting clinical trial design, monitoring, and implementation
  • Experience with study data readout activities
  • Experience contributing to regulatory submission documents

Work Rights

Not specified

Tailored Resume

Cover Letter