Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements
Job Summary
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
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 that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
Skills & Requirements
Must-have
Perform site monitoring visits
Evaluate study site practices
Manage study progress tracking
Maintain Investigator's Site File
Create study documentation
Collaborate with study team members
Nice-to-have
Adapt and drive subject recruitment
Support development of recruitment plan
Site financial management
Effective time and financial management
Key Requirements
At least 2 years on-site monitoring experience
Bachelor's Degree in scientific discipline or health care preferred
Good knowledge of clinical research regulatory requirements