Job Summary

• Manage the end-to-end delivery of study-specific informed consent forms (ICFs), ensuring they are high quality, compliant, and delivered on time.
• Review, edit, and contribute directly to ICF content to ensure accurate alignment with study protocols and regulatory requirements.
• Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities.

Matching Summary

Salary

Base: $129,233-159,079; Bonus/Equity: Discretionary annual bonus program, Stock-based long-term incentives; Benefits: Comprehensive employee benefits package, Retirement and Savings Plan, medical, dental, vision, life and disability insurance, flexible spending accounts

Skills & Requirements

Key Requirements

• Pharma and clinical trial processes expertise
• Global team structure experience
• Project management experience
• Doctorate degree OR Master’s degree & 2 years clinical trial experience
• Bachelor’s degree & 4 years clinical trial experience
• Associate’s degree & 8 years clinical trial experience
• High school diploma / GED & 10 years clinical trial experience

Work Rights