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 submissions, recruitment, CRF completion, and data query resolution, while ensuring site documentation is maintained according to GCP and local regulatory requirements.
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: $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
Site monitoring visits
Subject recruitment plan
Protocol and study training
Quality and integrity evaluation
Trial Master File (TMF) documentation
Good Clinical Practice (GCP)
ICH guidelines
Nice-to-have
Effective time management
Problem-solving skills
Establish effective working relationships
Financial management skills
Key Requirements
1 year on-site monitoring experience
Bachelor's Degree in scientific discipline or health care preferred
Knowledge of GCP and ICH guidelines
Proficiency in Microsoft Word, Excel, PowerPoint
Written and verbal communication skills in English