Description
We are seeking a Clinical Research Coordinator to join our team on a part-time basis for 24 hours a week, for a period of 6 months.
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.
Key responsibilities include:
- Pre-screening and recruitment support, including chart reviews, referral management, and community outreach
- Scheduling appointments, trial visits, labs, and scans as necessary
- Supporting patient education check-ins, pre-visit education, and pre-visit setup
- Verifying and correcting research study information on source documents, researching queries and variances, and providing feedback to the site data collector
- Accurate input of trial data into the Electronic Data Capture (EDC) system for recruitment
- Preparing and maintaining study files
- Scheduling visits with research subjects, generating appropriate reports and documentation
- Providing other administrative support functions such as reception, office organization, and supply management
To be successful in this role, you will need:
- A Bachelor's degree in life sciences
- Basic knowledge of clinical trials and study coordinator experience
- Availability to work part-time (24 hours per week)
- Availability to work in a fixed-term contract (6 months)
- Availability to work based in Curitiba, PR
IQVIA is committed to integrity in our hiring process and maintains a zero-tolerance policy for candidate fraud.