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: $71,900.00 - $169,300.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Range of health and welfare and/or other benefits
Skills & Requirements
Must-have
Onsite monitoring experience
Cardiovascular/Renal/Metabolic expertise
Oncology expertise
Neurology expertise
GCP and ICH guidelines
Site management and monitoring visits
Nice-to-have
Adapt subject recruitment plan
Effective time and financial management
Collaborate with study team members
Key Requirements
1-2 years onsite monitoring experience
Bachelor's Degree in scientific discipline or health care preferred
Basic knowledge of clinical research regulatory requirements
Proficiency in Microsoft Word, Excel and PowerPoint