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

539

Multiple Locations
$142,400.00 - $224,100.00; bonus + long-term incen...
Hybrid
End-to-end clinical supply chain
Clinical trial teams (ctt) participation
Sap system utilization
The Global Clinical Supply (GCS) organization manages the end-to-end integrated clinical supply chain for clinical trials, responsible for planning, sourcing, labeling, packaging, and delivery of clinical supplies globally

Job Summary

  • The Global Clinical Supply (GCS) organization manages the end-to-end integrated clinical supply chain for clinical trials, responsible for planning, sourcing, labeling, packaging, and delivery of clinical supplies globally.
  • The Protocol Clinical Supplies Project Manager serves as the primary GCS point of contact, participating in Clinical Trial Teams and product development meetings, and is accountable for establishing clinical supply timelines and providing sourcing signals.
  • The role requires strong analytical, problem-solving, and project management skills, with a focus on balancing strategy with tactical execution and making informed risk decisions.

Matching Summary

The Global Clinical Supply (GCS) organization manages the end-to-end integrated clinical supply chain for clinical trials, responsible for planning, sourcing, labeling, packaging, and delivery of clinical supplies globally.

Salary

$142,400.00 - $224,100.00; Bonus and long-term incentive eligible; Comprehensive benefits package

Skills & Requirements

Must-have

  • End-to-end clinical supply chain
  • Clinical Trial Teams (CTT) participation
  • SAP system utilization
  • Clinical supply documentation authoring
  • Risk analysis and mitigation strategies
  • Balancing patient needs and product supply

Nice-to-have

  • Continuous improvement mindset
  • Flexibility and adaptability
  • Strong ownership and accountability
  • Ethics and integrity
  • Focus on customers and patients

Key Requirements

  • Bachelor's degree required; MS/MBA preferred
  • At least 8 years of project management experience
  • At least 5 years of supply chain planning/coordination experience
  • Knowledge of early and late phase clinical trials
  • Excellent communication and interpersonal skills
  • Strong negotiation and influencing skills
  • Familiarity with supply chain systems (e.g., SAP)

Work Rights

Not specified

Tailored Resume

Cover Letter