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
Job Summary
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.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
Matching Summary
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.
Salary
Base: $64,000.00 - $189,000.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Range of health and welfare and/or other benefits
Skills & Requirements
Must-have
Perform site monitoring visits
Ensure protocol adherence
Track subject recruitment
Evaluate site quality
Manage study progress
Maintain Investigator's Site File
Nice-to-have
Drive predictability
Enhance predictability
Collaborate with study teams
Key Requirements
2.5 years clinical research coordination experience
Nursing or University Degree
Knowledge of electronic data capture preferred
Reside in the same country as job location
Work Rights
Must reside in the same country where the job is located