Clinical Research Professional: Flexible Opportunity in Brazil

Há 2 dias


São Paulo, São Paulo, Brasil IQVIA Argentina Tempo inteiro
About the Role

We are seeking a skilled Clinical Research Coordinator to join our team in São José dos Campos, Brazil. As a pivotal member of our site team, you will be responsible for supporting the smooth running of clinical trials and assisting with collecting patient data.

Key Responsibilities:
  • Verify and/or correct research study information on source documents;
  • Research queries and variances, providing feedback to the site data collector;
  • Accurately input trial data into the Electronic Data Capture (EDC) system and track visits and procedures completed against budget in the clinical trial management system (CTMS);
  • Prepare and maintain study files, ensuring timely submission of information;
  • Collect, submit, and assist in maintaining relevant regulatory and ethics documents;
  • Schedule visits with research subjects, generate reports, and documentation;
  • Provide administrative support functions such as reception, office organization, and supply management.
Requirements:
  • Bachelor's degree in life sciences;
  • Basic knowledge of clinical trials;
  • Basic knowledge of medical terminology;
  • Availability to work based in São José dos Campos;
  • Availability to work part-time (20 hours per week);
  • Availability to work in a fixed-term contract (6 months).
About IQVIA

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, improving patient outcomes and population health worldwide.



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