Clinical Trial Coord Ii

PPD (Thermo Fisher)

UK
Strong organizational skills
Attention to detail in documentation
Knowledge of ich gcp guidelines
The role involves providing administrative and technical support to ensure audit readiness and rapid site activations for global clinical trials

Job Summary

  • The role involves providing administrative and technical support to ensure audit readiness and rapid site activations for global clinical trials.
  • Candidates will coordinate file reviews, manage system databases like eTMF, and assist with regulatory submissions and feasibility activities.
  • The position requires maintaining knowledge of SOPs, client directives, and current regulatory guidelines while supporting the project team's critical path.

Matching Summary

The role involves providing administrative and technical support to ensure audit readiness and rapid site activations for global clinical trials.

Skills & Requirements

Must-have

  • Strong organizational skills
  • Attention to detail in documentation
  • Knowledge of ICH GCP guidelines
  • Proficiency in MS Office applications
  • Ability to manage multiple tasks

Nice-to-have

  • Self-motivated positive attitude
  • Effective oral communication skills
  • Good negotiation skills
  • Local language proficiency
  • Team collaboration abilities

Key Requirements

  • High school diploma or equivalent
  • Bachelor's degree preferred
  • 0 to 1 year relevant experience

Work Rights

Not specified

Tailored Resume

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