Cta1

IQVIA UK

Maintain clinical documents and systems
Prepare and file clinical documentation
Track and manage clinical data flow
Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines

Job Summary

  • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
  • Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Matching Summary

Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.

Skills & Requirements

Must-have

  • Maintain clinical documents and systems
  • Prepare and file clinical documentation
  • Track and manage clinical data flow
  • Communicate project correspondence
  • Working knowledge of Microsoft Office Suite

Nice-to-have

  • Awareness of GCP and ICH guidelines
  • Effective time management skills
  • Ability to maintain working relationships

Key Requirements

  • High School Diploma or equivalent
  • 3 years administrative support experience
  • Equivalent combination of education, training and experience
  • Written and verbal communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter