IQVIA is hiring Clinical Research Associates!
Join IQVIA today and make an impact on patients’ outcome!
Job Overview
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Responsibilities
- Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
- Supporting the development of a subject recruitment plan
- Establishing regular lines of communication plus administering protocol and related study training to assigned sites
- Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
Qualifications
- A Bachelor's degree in a health care or other scientific discipline or educational equivalent
- Experience in on-site monitoring of clinical trials
- Alternatively, you should have an equivalent combination of education, training and experience
- Written and verbal communication skills including good command of Polish and English language