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Salary
$20k – $50k per year (Estimated)
Location
In office (São Paulo)
Employment
Part-Time
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IQVIA is an American company formed in 2016 by the merger of the contract research organisation Quintiles, founded in 1982, with the pharmaceutical data business IMS Health. It runs clinical trials on behalf of drug and device makers and simultaneously operates one of the largest healthcare data estates in the world, covering prescriptions, claims and electronic medical records, which it sells back to the same industry for commercial planning and real-world evidence studies. Headquartered in Durham, North Carolina and listed on the New York Stock Exchange, it employs close to ninety thousand people and combines the trial and data businesses in what it calls connected intelligence.

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 periodof 6 months to support the site. The study coordinator should have experience clinically or nursing background as tasks includes perform EKG, collect vital signs.

This is an excellent opportunity if you have experience working as a SC

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
  • Basic knowledge of clinical trials, study coordinator experience
  • Availability to work based in Porto Alegre - RS
  • Availability 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.com

IQVIA 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.

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