Associate Director, Clinical Supplies Project Manager - Protocol (onsite)

Imsapharma Com Ar

Base: $142,400.00 - $224,100.00; bonus/equity: eli...
Hybrid
Clinical supply chain management
Project management
Sap system proficiency
The Global Clinical Supply organization manages the integrated clinical supply chain across the company's full portfolio of clinical trials, ensuring stable supply and balancing patient needs

Job Summary

  • The Global Clinical Supply organization manages the integrated clinical supply chain across the company's full portfolio of clinical trials, ensuring stable supply and balancing patient needs.
  • The role involves collaboration with clinical development, regulatory, quality, and supply chain teams to establish timelines, mitigate risks, and author clinical supply documentation.
  • The company offers a comprehensive benefits package including medical, dental, vision, retirement plans, paid holidays, vacation, and supports a hybrid work model for office-based U.S. employees.

Matching Summary

The Global Clinical Supply organization manages the integrated clinical supply chain across the company's full portfolio of clinical trials, ensuring stable supply and balancing patient needs.

Salary

Base: $142,400.00 - $224,100.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Medical, dental, vision, retirement, paid holidays, vacation, and more

Skills & Requirements

Must-have

  • Clinical supply chain management
  • Project management
  • SAP system proficiency
  • Clinical trial coordination
  • Change control processing
  • Cross-functional team collaboration

Nice-to-have

  • Data analytics and visualization
  • Continuous improvement mindset
  • Strong negotiation skills
  • Adaptability in dynamic environment
  • Customer and patient focus
  • Ethics and integrity

Key Requirements

  • Bachelor’s degree in scientific or business discipline
  • Minimum 8 years project management experience
  • Minimum 5 years supply chain planning experience
  • Knowledge of early and late phase clinical trials
  • Familiarity with GMP and GCP
  • Experience with ERP systems such as SAP
  • Excellent communication and interpersonal skills

Work Rights

US and Puerto Rico Residents Only

Tailored Resume

Cover Letter