Site Activation Coordinator

IQVIA UK

Buenos Aires, Argentina
Site activation activities
Regulatory documents review
Clinical trial environment awareness
Perform tasks at a country level associated with site activation 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 activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines.
  • Review documents for completeness, consistency and accuracy, under guidance of senior staff, and prepare site regulatory documents.
  • Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.

Matching Summary

Perform tasks at a country level associated with site activation 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
  • regulatory documents review
  • clinical trial environment awareness
  • updating internal systems

Nice-to-have

  • interpersonal communication skills
  • organizational skills
  • ability to work on multiple projects
  • effective working relationships

Key Requirements

  • Bachelor's Degree Life sciences
  • 1 years’ experience healthcare environment
  • Advanced English level

Work Rights

Not specified

Tailored Resume

Cover Letter