Clinical Research Coordinator -Centro Integrado de Pesquisa _ São José do Rio Preto Full time & Fix Term

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 initially for a period of 8 months to support the 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:

• BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession 

• Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules

• Basic knowledge of medical terminology

• Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word

• Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client

• ​Good organizational skills with the ability to pay close attention to detail.

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.