Perform monitoring and site management work to ensure sites conduct studies and report data as required by the study 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 study protocol, regulations, and sponsor requirements.
Evaluate the quality and integrity of study site practices, manage study progress, and ensure proper documentation for filing in the Trial Master File (TMF) and Investigator's Site File (ISF).
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 sites conduct studies and report data as required by the study protocol, regulations, and sponsor requirements.
Skills & Requirements
Must-have
Perform site monitoring visits
Ensure adherence to GCP and ICH guidelines
Manage study progress and data queries
Maintain Trial Master File (TMF) and Investigator's Site File (ISF)
Written and verbal communication skills
Nice-to-have
Establish effective working relationships
Drive and track subject recruitment
Collaborate with study team members
Key Requirements
Bachelor's Degree in scientific discipline or health care preferred
Prior on-site monitoring experience
Basic knowledge of clinical research regulatory requirements