# Clinical Research Coordinator

**Company**: IQVIA
**Location**: Curitiba, PR
**Work arrangement**: onsite
**Experience**: entry
**Job type**: part-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Clinical-Research-Coordinator---Curitiba---Part-Time---Fix-Term-_R1561535?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_7b600907-bc4

## 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.

## Skills

### Required
- life sciences
- clinical trials
- study coordinator

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/So-Paulo-Brazil/Clinical-Research-Coordinator---Curitiba---Part-Time---Fix-Term-_R1561535?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)