Senior Clinical Study Administrator - Luton, Uk (hybrid) - Fsp

Parexel

Luton, United Kingdom
Senior clinical study administrator role
Fluent in french language required
3 days per week onsite at sponsor office
This role involves coordinating clinical study activities from start-up to close-out while ensuring quality and consistency of deliverables

Job Summary

  • This role involves coordinating clinical study activities from start-up to close-out while ensuring quality and consistency of deliverables.
  • The position requires a hybrid work model with mandatory attendance at the sponsor's office in Luton for at least three days per week.
  • Parexel offers opportunities for professional development within a team dedicated to improving global health through clinical trials.

Matching Summary

This role involves coordinating clinical study activities from start-up to close-out while ensuring quality and consistency of deliverables.

Skills & Requirements

Must-have

  • Senior Clinical Study Administrator role
  • Fluent in French language required
  • 3 days per week onsite at sponsor office
  • ICH-GCP guidelines knowledge
  • eTMF and ISF document management
  • CTMS system proficiency (VCV, SharePoint)
  • Regulatory submission support

Nice-to-have

  • Previous medical or life science admin experience
  • Ability to train others on procedures
  • Experience with top 50 Pharma sponsors
  • Strong interpersonal skills for international teams
  • High ethical standards and integrity

Key Requirements

  • Degree supporting position skills
  • Proficient written and spoken English
  • Fluent French language skills
  • Understanding of ICH-GCP guidelines
  • Administrative experience in medical field preferred

Work Rights

Not specified

Tailored Resume

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