Clinical Trials Assistant With Finance Responsibilities Sponsor-dedicated

IQVIA UK

Riyadh, Saudi Arabia
Trial master file management
Clinical documentation handling
Clinical data flow coordination
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.
  • Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
  • 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

  • Trial Master File management
  • clinical documentation handling
  • clinical data flow coordination
  • project communications
  • Arabic and English language proficiency

Nice-to-have

  • effective time management
  • organizational skills
  • establish working relationships

Key Requirements

  • High School Diploma or equivalent
  • At least 1 year experience as CTA
  • Finance responsibilities
  • Experience in contracts, payments, budgeting, invoicing
  • Minimum one year clinical research experience
  • Computer skills (Word, Excel, PowerPoint)
  • Basic knowledge of GCP and ICH guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter