IQVIA CRA Jobs Brazil – Apply Online
Discover unparalleled career opportunities with IQVIA, a global leader in clinical research services. This article explores the CRA 1 role in São Paulo, Brazil—detailing essential functions, qualifications, and how you can be part of innovative healthcare advancements that improve patient outcomes worldwide.
Job Overview
Perform monitoring and site management work to ensure that sites conduct the studies and report study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Essential Functions
- Perform site monitoring visits in accordance with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Work with sites to drive subject recruitment plan in line with project needs.
- Administer protocol and study training to assigned sites.
- Evaluate the quality and integrity of study site practices.
- Manage the progress of assigned studies by tracking regulatory submissions, recruitment, enrollment, and data query resolution.
- Ensure site documents are available for filing in the Trial Master File (TMF).
- Create and maintain documentation regarding site management.
- Collaborate with study team members for project execution support.
- May be accountable for supporting development of project subject recruitment plan and site financial management.
Qualifications
- Bachelor’s Degree in scientific discipline or health care preferred.
- Minimum 1 year of on-site monitoring experience.
- Good knowledge of GCP and ICH guidelines.
- Computer skills including proficiency in Microsoft Word, Excel, and PowerPoint.
- Written and verbal communication skills with good command of English.
Keywords: IQVIA, CRA, São Paulo, Brazil, Clinical Research, GCP, ICH, Monitoring, Site Management
