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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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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. Learn more at https://jobs.iqvia.com