Clinical Trial Assistant 2

IQVIA UK

Guatemala City, Guatemala
Clinical research experience
Knowledge of gcp/ich guidelines
Ability to manage multiple projects
Perform tasks associated with Site Activation activities in accordance with regulations and project requirements

Job Summary

  • Perform tasks associated with Site Activation activities in accordance with regulations and project requirements.
  • Serve as Single Point of Contact for investigative sites and project teams.
  • Ensure adherence to SOPs and maintain project timelines.

Matching Summary

Perform tasks associated with Site Activation activities in accordance with regulations and project requirements.

Skills & Requirements

Must-have

  • Clinical research experience
  • Knowledge of GCP/ICH guidelines
  • Ability to manage multiple projects

Nice-to-have

  • Effective communication skills
  • Good negotiating skills
  • Ability to work independently

Key Requirements

  • Bachelor's Degree in life sciences
  • 1 - 2 years clinical research experience
  • Fluent English

Work Rights

Not specified

Tailored Resume

Cover Letter