Senior/clinical Research Associate(beijing/shanghai/guangzhou/other Cities)
IQVIA UK
Beijing, China
Perform site monitoring visits
Ensure site compliance with regulations
Manage study progress tracking
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.
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
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
ensure site compliance with regulations
manage study progress tracking
maintain site documentation
collaborate with study team members
Nice-to-have
adapt subject recruitment plan
support project execution
effective time management skills
problem-solving skills
Key Requirements
at least 1 year on-site monitoring experience
Bachelor's Degree in scientific discipline or health care preferred
Good Clinical Practice (GCP) and ICH guidelines knowledge