Sr Ctm - Cell And Gene Therapy France/belgium - Fsp

PPD (Thermo Fisher) UK

France/Belgium
Not specified; not specified; not specified
Fully remote
Fluency in english dutch and french
3+ years ctm experience
Ich-gcp and local regulation compliance
This role leads local study teams to deliver clinical study components according to agreed resources, budget, and timelines while ensuring compliance with ICH-GCP

Job Summary

  • This role leads local study teams to deliver clinical study components according to agreed resources, budget, and timelines while ensuring compliance with ICH-GCP.
  • The position is responsible for the full lifecycle of site management including identification, qualification, initiation, monitoring, closure, and documentation archiving.
  • Joining this FSP functional area allows you to work within the renowned PPD CRO while gaining invaluable client-dedicated experience in a global mission to improve health outcomes.

Matching Summary

This role leads local study teams to deliver clinical study components according to agreed resources, budget, and timelines while ensuring compliance with ICH-GCP.

Salary

Not specified; Not specified; Not specified

Skills & Requirements

Must-have

  • Fluency in English Dutch and French
  • 3+ years CTM experience
  • ICH-GCP and local regulation compliance
  • Site identification and qualification management
  • Local study team leadership

Nice-to-have

  • Strong project management approach
  • Matrix team environment experience
  • Risk management plan development
  • Digital innovation adoption
  • Conflict resolution skills

Key Requirements

  • Bachelor's degree or equivalent
  • 3+ years Clinical Trial Manager experience
  • Fluent in English, Dutch, and French
  • Experience in site monitoring

Work Rights

Not specified

Tailored Resume

Cover Letter