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: $57,500.00 - $226,800.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Range of health and welfare and/or other benefits
Skills & Requirements
Must-have
Site monitoring visits
Subject recruitment plan
Protocol and study training
Quality and integrity evaluation
Trial Master File (TMF)
Investigator's Site File (ISF)
Nice-to-have
Effective time management
Problem-solving skills
Client relationship management
Key Requirements
1.5 years on-site monitoring experience
Bachelor's Degree in scientific discipline or health care preferred
Good Clinical Practice (GCP)
International Conference on Harmonization (ICH) guidelines
Proficiency in Microsoft Word, Excel and PowerPoint