Cta1

IQVIA

Hong Kong, Hong Kong
Clinical document management
Trial master file maintenance
Clinical trial supplies tracking
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries

Job Summary

  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
  • The role involves assisting clinical teams with preparation, handling, distribution, filing, and archiving of clinical documentation according to standard operating procedures.
  • The position requires acting as a central contact for clinical project communications and may include accompanying Clinical Research Associates on site visits after training.

Matching Summary

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Skills & Requirements

Must-have

  • Clinical document management
  • Trial Master File maintenance
  • Clinical Trial Supplies tracking
  • Case Report Forms management
  • Microsoft Word, Excel, PowerPoint
  • Good Clinical Practice awareness
  • Effective time management

Nice-to-have

  • Written and verbal communication skills
  • Organizational skills
  • Ability to maintain effective working relationships
  • Knowledge of protocol requirements
  • Clinical monitoring assistance

Key Requirements

  • High School Diploma or equivalent
  • 3 years administrative support experience
  • Awareness of Good Clinical Practice (GCP) and ICH guidelines
  • Equivalent combination of education, training and experience

Work Rights

Not specified

Tailored Resume

Cover Letter