Clinical Research Coordinator in Porto Alegre, Brazil

Há 4 dias

São Paulo, Brasil IQVIA Tempo inteiro

Clinical Research Coordinator in Porto Alegre, Brazil (Fixed term & Part time)

IQVIA is looking for a Clinical Research Coordinator in Porto Alegre, Brazil. This is a fixed-term, part-time role (24 hours per week) with an initial 6-month contract and an immediate start to support the site. The role involves administrative tasks to support investigators and assist with collecting patient data; the coordinator should have a clinical or nursing background and may perform tasks such as EKG and collecting vital signs.

Responsibilities
  • Verifying and/or correcting research study information on source documents; researching queries and variances; providing feedback to the site data collector
  • Accurate input of trial data into the Electronic Data Capture (EDC) system and tracking visits and procedures completed against budget in the clinical trial management system (CTMS)
  • Preparing and maintaining study files, and timely submission of information
  • Collecting, submitting and assisting in maintaining relevant regulatory and ethics documents
  • Scheduling visits with research subjects, generating appropriate reports and documentation
  • Other administrative support functions such as reception, office organization and supply management
Qualifications
  • Bachelor's degree in life sciences
  • Basic knowledge of clinical trials, experience as study coordinator
  • Availability to work based in Porto Alegre, Rio Grande do Sul, Brazil
  • Availability to work part-time (24 hours per week)
  • Availability to work in a fixed-term contract (6 months)

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

Note: This description retains the original role context and requirements without translation or addition of new information.

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