Clinical Research Coordinator - Joinville - SC - Part Time Fix Term

IQVIA; São Paulo; Presencial; BRL 80.000 - 120.000; Tempo parcial

Resumo da oferta

A leading clinical research organization is seeking a Clinical Research Coordinator for an immediate start in São Paulo, Brazil. This part-time role (20 hours a week) will last for 6 months and requires a Bachelor's degree in life sciences along with experience in clinical trials. Responsibilities include supporting patient recruitment, scheduling appointments, and managing study files. This opportunity offers flexible working arrangements with a focus on career development and contribution to improving patient outcomes.

Serviços

Flexible working arrangements

Career progression opportunities

Qualificações

• Experience in clinical trials or nursing background.
• Ability to perform EKG and collect vital signs.
• Availability to work 20 hours per week for 6 months.

Responsabilidades

• Pre-screening and recruitment support including chart reviews.
• Schedule appointments and visit reminder calls.
• Accurate input of trial data into the EDC system.

Conhecimentos

Clinical research knowledge

Patient education

Chart review

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. 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:

• Pre-screening & recruitment support including chart reviews. (referralmanagement and community outreach)
• Schedule appointments (trial visits, labs, Scans if appropriate) and Visit/Activity reminder calls
• Support Patient Education check-ins, pre visit education , pre visit setup
• 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 for recruitment
• Preparing and maintaining study files
• 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 Joinville - SC
• Availability to work part-time (20 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