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.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
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
Manage study progress
Maintain Investigator's Site File
Create site documentation
Nice-to-have
Adapt subject recruitment plan
Support start-up phase
Site financial management
Key Requirements
2.5 years clinical research coordination experience
Nursing or University Degree
Knowledge of electronic data capture preferred
Work Rights
Must reside in the same country where the job is located