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 are looking Clinical Research Coordinator.This role has an immediate start working 24 hours a week for a period of 6 months to support the site.This is an excellent opportunity if you have experience working as a SCAs 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:Pre-screening & recruitment support including chart reviews. (referralmanagement and community outreach)Schedule appointments (trial visits, labs, Scans if appropriate) and Visit/Activity reminder callsSupport Patient Education check-ins, pre visit education , pre visit setupVerifying and/or correcting research study information on source documents; researching queries and variances; providing feedback to the site data collectorAccurate input of trial data into the Electronic Data Capture (EDC) system for recruitmentPreparing and maintaining study filesScheduling visits with research subjects, generating appropriate reports and documentationOther 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 sciencesBasic knowledge of clinical trials, study coordinator experienceAvailability to work based in Curitiba PRAvailability 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. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.