Global Study Manager

GSK

Mississauga, Ontario, Canada
Cad117,000 to cad167,000; not specified; not speci...
Hybrid (2-3 days onsite)
Global study management
Clinical operations delivery
Vendor oversight and management
GSK is seeking a Global Study Manager in Mississauga, Ontario, to oversee clinical operations from study initiation to archiving, ensuring adherence to timelines and quality standards. The ideal candidate will possess extensive experience in clinical research and project management, along with strong leadership and communication skills

Job Summary

  • The Global Study Manager (GSM) will own the creation of robust, accelerated delivery plans to ensure timelines, quality standards, and ambitious targets are consistently achieved for assigned clinical studies.
  • This role involves leading the Operational Working Group for in-house studies and actively participating as a key member of the Central Study Team (CST) to ensure seamless end-to-end study delivery.
  • GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, uniting science, technology, and talent to get ahead of disease together.

Matching Summary

Match Score: 85

GSK is seeking a Global Study Manager in Mississauga, Ontario, to oversee clinical operations from study initiation to archiving, ensuring adherence to timelines and quality standards. The ideal candidate will possess extensive experience in clinical research and project management, along with strong leadership and communication skills.

Salary

CAD117,000 to CAD167,000; Not specified; Not specified

Skills & Requirements

Must-have

  • Global Study Management
  • Clinical Operations Delivery
  • Vendor Oversight and Management
  • ICH/GCP Compliance
  • Risk Management and Mitigation
  • Matrix Team Leadership

Nice-to-have

  • Innovative approaches to study delivery
  • Cross-functional collaboration
  • Adaptability to change and uncertainty
  • Multicultural experience

Key Requirements

  • Bachelor's degree in life sciences or related discipline
  • In-depth experience in clinical research study management
  • Strong project management skills and tools experience
  • Experience across multiple study designs
  • In-depth knowledge of GCPs and ICH guidelines
  • Excellent stakeholder management and communication skills
  • Demonstrated leadership skills
  • Ability to manage competing priorities in a global environment

Work Rights

Not specified

Tailored Resume

Cover Letter