Senior/clinical Research Associate(beijing/shanghai/guangzhou/other Cities)
IQVIA Inc
Beijing, China
Site monitoring visits
Subject recruitment plan
Protocol and study training
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
site monitoring visits
subject recruitment plan
protocol and study training
quality and integrity evaluation
study progress management
Trial Master File (TMF) documentation
site management documentation
Nice-to-have
collaboration with study team
development of recruitment plan
site financial management
Key Requirements
at least 1 year of on-site monitoring experience
Bachelor's Degree in scientific discipline or health care preferred