Clinical Research Coordinator, IPECC, Campinas (Full-time/Fixed-Term)

IQVIA LLC; Brasil; Teletrabalho; BRL 60 000 - 90 000; Tempo parcial

Resumo da oferta

IQVIA LLC is seeking a Clinical Research Coordinator for an on-site, six-month contract in Campinas. The role supports investigators, performs EKGs and vital signs, and handles data collection and study administration on a daily basis.

The candidate should have a nursing or clinical background with life sciences credentials and be able to work 40 hours per week in a fixed-term position, ensuring smooth trial operations at the site.

Qualificações

• Bachelor's degree in life sciences is required.
• Previous experience as Study Coordinator.
• Basic knowledge of medical terminology.
• Experience performing EKG and collecting vital signs.
• Based in Campinas.
• Availability to work part-time (40 hours per week).
• Fixed-term contract through March 2027.

Responsabilidades

• 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 EDC system and tracking visits and procedures in CTMS.
• Preparing and maintaining study files and timely submission of information.
• Collecting, submitting and maintaining regulatory and ethics documents.
• Scheduling visits with research subjects and generating reports.

Conhecimentos

Study Coordinator

Medical terminology

EKG

Vital signs

Campinas location

Fortnightly start

Formação académica

Bachelor's degree in life sciences

Ferramentas

EDC system

CTMS

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 40 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

• 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.

Required skills and experience

• Bachelor's degree in life sciences;
• Previous experience as Study Coordinator;
• Basic knowledge of medical terminology;
• Experience performing EKG and collecting vital signs;
• Availability to work based in Campinas;
• Availability to work part-time (40 hours per week);
• Availability to work in a fixed term contract (6 months), until March2027.

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. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.