IQVIA is seeking a Sr. CRA in Taipei, Taiwan, responsible for site monitoring and management in clinical research. The ideal candidate should have at least two years of on-site monitoring experience and possess knowledge of Good Clinical Practice and relevant regulatory requirements
Job Summary
Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations.
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Matching Summary
Match Score: 85
IQVIA is seeking a Sr. CRA in Taipei, Taiwan, responsible for site monitoring and management in clinical research. The ideal candidate should have at least two years of on-site monitoring experience and possess knowledge of Good Clinical Practice and relevant regulatory requirements.
Skills & Requirements
Must-have
site monitoring visits
subject recruitment plan
protocol and study training
quality and integrity evaluation
trial master file documentation
site management documentation
Nice-to-have
effective time management
effective financial management
establish working relationships
Key Requirements
at least 2 years of on-site monitoring experience
Good Clinical Practice (GCP) and ICH guidelines
Computer skills including Microsoft Word, Excel and PowerPoint