IQVIA UK is seeking a Senior Clinical Research Associate (Sr. CRA) in Panama City, Panama, to oversee site monitoring and management in clinical studies. The role requires at least 4 years of on-site monitoring experience and strong communication and organizational skills
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 UK is seeking a Senior Clinical Research Associate (Sr. CRA) in Panama City, Panama, to oversee site monitoring and management in clinical studies. The role requires at least 4 years of on-site monitoring experience and strong communication and organizational skills.
Skills & Requirements
Must-have
site monitoring visits
subject recruitment plan
protocol and study training
quality and integrity evaluation
trial master file (TMF)
investigator's site file (ISF)
study documentation
Nice-to-have
collaboration with study team
site financial management
Key Requirements
Bachelor's Degree in scientific discipline or health care