Perform monitoring and site management work to ensure sites are conducting studies and reporting data as required by protocol, regulations, and sponsor requirements
Job Summary
Perform monitoring and site management work to ensure sites are conducting studies and reporting data as required by protocol, regulations, and sponsor requirements.
Manage the progress of assigned studies by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
Matching Summary
Perform monitoring and site management work to ensure sites are conducting studies and reporting data as required by protocol, regulations, and sponsor requirements.
Skills & Requirements
Must-have
Perform site monitoring visits
Evaluate study site practices
Manage study progress
Maintain Trial Master File
Site financial management
Nice-to-have
Drive subject recruitment plan
Establish communication with sites
Collaborate with study team members
Key Requirements
1 year on-site monitoring experience
Good Clinical Practice (GCP) knowledge
International Conference on Harmonization (ICH) guidelines knowledge