Clinical Trial Assistant 1 - Sponsor Dedicated- Prague

IQVIA

Prague, Czech Republic
Trial master file (tmf) maintenance
Clinical documentation handling
Study file completeness review
As Clinical Trial Assistant, you will be working in our Clinical Trials Team together with some of the most talented people in the field and gain a brought knowledge in the execution of clinical trials

Job Summary

  • As Clinical Trial Assistant, you will be working in our Clinical Trials Team together with some of the most talented people in the field and gain a brought knowledge in the execution of clinical trials.
  • Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
  • We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available.

Matching Summary

As Clinical Trial Assistant, you will be working in our Clinical Trials Team together with some of the most talented people in the field and gain a brought knowledge in the execution of clinical trials.

Skills & Requirements

Must-have

  • Trial Master File (TMF) maintenance
  • Clinical documentation handling
  • Study file completeness review
  • Clinical Trial Supplies management
  • CRF and data flow tracking
  • Project communication coordination

Nice-to-have

  • Talented people in the field
  • Vast career development opportunities
  • Effective time management skills
  • Ability to establish relationships

Key Requirements

  • Bachelor's Degree in Science
  • Previous experience as Trainee (Clinical Trials), CTA, or Coordinator
  • Computer skills (Word, Excel, PowerPoint)
  • Written and verbal Czech and English skills
  • Awareness of GCP and ICH guidelines
  • Knowledge of applicable protocol requirements

Work Rights

Not specified

Tailored Resume

Cover Letter