Job Overview
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. Essential Functions Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH…
What you'll do
- Perform site monitoring visits including selection, initiation, monitoring and close-out visits
- Ensure sites conduct studies in accordance with study protocol
- Verify study data reporting meets requirements
- Ensure compliance with applicable regulations and guidelines
- Ensure compliance with sponsor requirements
- Perform site management work
What you'll need
- Knowledge of Good Clinical Practice (GCP) guidelines
- Understanding of International Conference on Harmonization (ICH) standards
- Familiarity with study protocols and regulatory requirements
- Ability to conduct site monitoring visits
- Knowledge of sponsor requirements and guidelines
About the Company
IQ