Clinical Supplies Manager

Summit Therapeutics Inc.

Remote
$120,000—$145,000 usd py
Remote
Clinical trial supply planning
Vendor management
Inventory management systems
Summit Therapeutics Inc. is seeking a Clinical Supplies Manager to enhance their supply chain strategy for clinical development in oncology. The role involves planning, vendor management, and ensuring compliance with regulatory standards, requiring a candidate with significant experience in clinical supplies management within a pharmaceutical or biotech environment

Job Summary

  • The Clinical Supply Manager will be responsible for planning and execution of operations for their assigned clinical supply projects and to support the ongoing development pipeline as well as optimization of Clinical Supplies department processes.
  • The candidate must have demonstrated effective collaborative skills to work across various phases of clinical development and serve as a key supply chain expert for cross functional teams.
  • Summit Therapeutics Inc. is a biopharmaceutical oncology company with a mission focused on improving quality of life, increasing potential duration of life, and resolving serious unmet medical needs.

Matching Summary

Match Score: 85

Summit Therapeutics Inc. is seeking a Clinical Supplies Manager to enhance their supply chain strategy for clinical development in oncology. The role involves planning, vendor management, and ensuring compliance with regulatory standards, requiring a candidate with significant experience in clinical supplies management within a pharmaceutical or biotech environment.

Salary

$120,000—$145,000 USD

Skills & Requirements

Must-have

  • Clinical trial supply planning
  • Vendor management
  • Inventory management systems
  • Regulatory compliance
  • Risk management
  • Cross-functional collaboration

Nice-to-have

  • Agile organization
  • Innovative solutions
  • Global workgroup associates

Key Requirements

  • Bachelor's degree in relevant discipline
  • Minimum 5 years' experience in Supplies management
  • Proficiency in relevant software applications
  • Experience managing complex international clinical studies
  • Understanding of regulatory and GMP requirements

Work Rights

Not specified

Tailored Resume

Cover Letter