Global Study Manager

GSK

Base: cad117,000 to cad167,000; bonus/equity: not ...
Hybrid (2-3 days onsite)
Clinical operations delivery
Study initiation and archiving
Vendor oversight and management
GSK is seeking a Global Study Manager to oversee the clinical operations of assigned studies, ensuring timely and quality delivery while adhering to regulatory standards. The role requires strong project management skills and offers an opportunity to contribute significantly to GSK's mission of impacting global health

Job Summary

  • This role within GCSD plays a pivotal part in driving the clinical operations of assigned studies, from Commit to Study Initiation (CSI) all the way through to study archiving.
  • As a Global Study Manager (GSM), you'll take ownership of crafting robust, accelerated delivery plans that aim for top-tier performance—ensuring timelines, quality standards, and ambitious targets are consistently achieved.
  • This role follows GSK’s Performance with Choice flexible‑working approach—balancing individual flexibility with team collaboration—and requires on‑site attendance 2–3 days per week to support core team activities and business needs.

Matching Summary

Match Score: 85

GSK is seeking a Global Study Manager to oversee the clinical operations of assigned studies, ensuring timely and quality delivery while adhering to regulatory standards. The role requires strong project management skills and offers an opportunity to contribute significantly to GSK's mission of impacting global health.

Salary

Base: CAD117,000 to CAD167,000; Bonus/Equity: Not specified; Benefits: Not specified

Skills & Requirements

Must-have

  • Clinical operations delivery
  • Study initiation and archiving
  • 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
  • Curious, accountable, and collaborative culture

Key Requirements

  • Bachelor’s degree in life sciences or related discipline
  • In-depth experience in clinical research study management
  • Strong project management skills
  • Experience with multiple study designs
  • In-depth knowledge of GCPs and ICH guidelines
  • Demonstrated leadership skills
  • Experience in multicultural settings

Work Rights

Not specified

Tailored Resume

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