Clinical Research Coordinator - Porto Alegre - Part Time Fix Term

IQVIA UK

Porto Alegre, Brazil
Perform ekg
Collect vital signs
Input trial data
This role has an immediate start working 24 hours a week for a period of 6 months to support the site

Job Summary

  • This role has an immediate start working 24 hours a week for a period of 6 months to support the site.
  • Day to day responsibilities will include: Verifying and/or correcting research study information on source documents; researching queries and variances; providing feedback to the site data collector.
  • We are looking for candidates with the following skills and experience: Bachelor's degree in life sciences Basic knowledge of clinical trials, study coordinator experience.

Matching Summary

This role has an immediate start working 24 hours a week for a period of 6 months to support the site.

Skills & Requirements

Must-have

  • perform EKG
  • collect vital signs
  • input trial data
  • maintain study files
  • schedule research visits

Nice-to-have

  • career progression support
  • flexible working options
  • industry leading company

Key Requirements

  • Bachelor's degree in life sciences
  • Basic knowledge of clinical trials
  • Study coordinator experience
  • Availability to work based in Porto Alegre - RS
  • Availability to work part-time (24 hours per week)
  • Availability to work in a fixed term contract (6 months)

Work Rights

Not specified

Tailored Resume

Cover Letter