Research Coordinator in SP, ABC region, Brazil (Fixed-Term & Part-time)Are you looking for an opportunity in Clinical Research?
Do you want to work for an industry-leading company that offers you experience and supports career progression whilst giving you the option of working flexibly?
If so, come and join us - IQVIA is looking for a Clinical Research Coordinator.
This role has an immediate start working 24 hours a week for a period of 4 months to support the site and work every day on site.
The study coordinator should have a clinically experienced or nursing background as tasks include performing EKGs and collecting vital signs.
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.
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.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.We are looking for candidates with the following skills and experience: Bachelor's degree in life sciences.Previous experience as Study Coordinator.Basic knowledge of medical terminology.Availability to work based in Fortaleza, Ceará.Availability to work part-time (20 hours per week).Availability to work in a fixed-term contract (6 months).
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