Clinical Trial Assistant 2

IQVIA

Guatemala City, Guatemala
Site activation activities
Investigative site communication
Regulatory document preparation
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines

Job Summary

  • Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.
  • Serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.
  • Provide local expertise to SAMs and project team during initial and on-going project timeline planning.

Matching Summary

Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.

Skills & Requirements

Must-have

  • Site Activation activities
  • Investigative site communication
  • Regulatory document preparation
  • Clinical systems maintenance
  • GCP/ICH guidelines knowledge

Nice-to-have

  • Negotiating and communication skills
  • Ability to challenge
  • Effective prioritization
  • Team collaboration

Key Requirements

  • Bachelor's Degree in life sciences
  • 1-2 years clinical research experience
  • Fluent English
  • Knowledge of applicable regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter