Clinical Research Coordinator - Goiânia - Part Time Fix Term

Iqvia; São Paulo; Presencial; BRL 36 000 - 60 000; Tempo parcial

Resumo da oferta

IQVIA in Goiânia is seeking a Clinical Research Coordinator to support investigators and ensure smooth running of trials.

The role is part-time, 24 hours per week, with an initial 6-month contract. You will handle pre-screening, scheduling visits, data entry, and site coordination.

Candidates should have a life sciences degree and study coordinator experience, with willingness to work in Goiás state.

Qualificações

• Bachelor's degree in life sciences.
• Basic knowledge of clinical trials.
• Availability to work based in Goiânia.

Responsabilidades

• Pre-screening & recruitment support including chart reviews.
• Schedule visits, labs, and reminder calls.
• Verifying and inputting trial data into the EDC system.
• Preparing and maintaining study files and documentation.
• Other admin support such as reception and supply management.

Conhecimentos

Clinical trials knowledge

Study coordinator experience

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 24 hours a week for a period of 6 months to support the site.

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. (referral management 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 Goiânia
• 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.