Senior Clinical Trial Manager

Galderma

Multiple Locations
Base: $170,000-$190,000; bonus/equity: annual shor...
Hybrid
Global clinical trial management
Budget and timeline management
Vendor management (cros/fsps)
The Senior CTM plans and manages overall activities for assigned global clinical trial(s), including timelines, budgets, resources, investigational sites, vendors, and key deliverables, ensuring compliance with SOPs, regulatory requirements, and ICH/GCP guidelines

Job Summary

  • The Senior CTM plans and manages overall activities for assigned global clinical trial(s), including timelines, budgets, resources, investigational sites, vendors, and key deliverables, ensuring compliance with SOPs, regulatory requirements, and ICH/GCP guidelines.
  • Essential functions include leading and managing cross-functional Clinical Trial Teams, establishing project milestones and budgets, managing clinical trial progress, proactively identifying risks, and contributing to regulatory submissions.
  • Galderma offers a competitive compensation package including base salary, annual short-term incentive program, comprehensive benefits, generous paid time off, and hybrid work schedules.

Matching Summary

The Senior CTM plans and manages overall activities for assigned global clinical trial(s), including timelines, budgets, resources, investigational sites, vendors, and key deliverables, ensuring compliance with SOPs, regulatory requirements, and ICH/GCP guidelines.

Salary

Base: $170,000-$190,000; Bonus/Equity: annual short-term incentive program; Benefits: health insurance, 401(k) plan with employer match, generous paid time off

Skills & Requirements

Must-have

  • Global clinical trial management
  • Budget and timeline management
  • Vendor management (CROs/FSPs)
  • ICH/GCP compliance
  • Cross-functional team leadership

Nice-to-have

  • Advancing dermatology for every skin story
  • Focus on results and positive energy
  • Passion for meaningful work
  • Embrace diversity and inclusion

Key Requirements

  • University degree in Life Sciences
  • 5+ years progressive experience in clinical research/operations
  • Experience managing clinical trials in major markets (US, China)
  • Experience supervising CROs
  • Excellent understanding of drug development process
  • Excellent knowledge of ICH/GCP guidelines
  • Fluent in English (written and oral)

Work Rights

Not specified

Tailored Resume

Cover Letter