Clinical Research Coordinator, Centro de Pesquisas em Diabetes e Doenças Endocrino - Metabolica[...]

IQVIA; São Paulo; Presencial; BRL 20.000 - 80.000; Tempo parcial

Resumo da oferta

IQVIA is seeking a Clinical Research Coordinator for an immediate part-time role (20 hours/week) for 6 months in São Paulo. The position involves supporting clinical trials through data management, administrative tasks, and regulatory submissions, ideal for candidates with a life sciences background.

Qualificações

• Previous experience as Study Coordinator.
• Availability to work part-time (20 hours per week).
• Availability to work in a fixed-term contract (6 months).

Responsabilidades

• Accurate input of trial data into the EDC system.
• Preparing and maintaining study files.
• Scheduling visits with research subjects.

Conhecimentos

Basic knowledge of medical terminology

Formação académica

Bachelor's degree in life sciences

Descrição da oferta de emprego

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 20 hours a week for a period of 6 months to support the site and work every day on site. The study coordinator should have experience clinically or nursing background as tasks includes perform EKG, collect vital signs.

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) from Monday to Friday

• Availability to work in a fixed term contract (6 months, until November 2025).

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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