Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor requirements
Job Summary
Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor requirements.
Manage study progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence.
Matching Summary
Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, 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 and drive subject recruitment
Evaluate site quality and integrity
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