$101,600.00 - $169,300.00; not specified; not spec...
On-site monitoring experience
Site management
Subject recruitment plan
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, and ensure proper documentation for the Trial Master File and Investigator's Site File.
IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence, creating intelligent connections 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
$101,600.00 - $169,300.00; Not specified; Not specified
Skills & Requirements
Must-have
On-site monitoring experience
Site management
Subject recruitment plan
Protocol and study training
Quality and integrity evaluation
Trial Master File (TMF) filing
Nice-to-have
Therapeutic area knowledge
Cross-functional collaboration
Key Requirements
At least 2 years of on-site monitoring experience
Bachelor's Degree in scientific discipline or health care preferred
Good Clinical Practice (GCP) and ICH guidelines knowledge
Equivalent combination of education, training and experience may be accepted