Vaga de Clinical Research Coordinator -Sao Luis_ Maranhao _ BRAZIL
1 vaga: | Publicada em 17/05
- A Combinar
Sobre a vaga
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.
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.
.
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 advanced analytics, technology solutions and
clinical research services to the life sciences industry. We believe in pushing
the boundaries of human science and data science to make the biggest impact
possible to help our customers create a healthier world. Learn more at
https://jobs.iqvia.com