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.
Evaluate the quality and integrity of study site practices, manage study progress, and ensure proper documentation for the Trial Master File.
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence, aiming to accelerate the development and commercialization of innovative medical treatments.
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: $47,400.00 - $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
Perform site monitoring visits
Ensure protocol adherence
Manage study progress
Maintain Investigator's Site File
Good Clinical Practice (GCP)
ICH guidelines
Nice-to-have
Enhance predictability of recruitment
Effective time management skills
Effective financial management skills
Establish effective working relationships
Key Requirements
Bachelor's Degree in scientific discipline or health care preferred