Experienced Clinical Research Associate - Sponsor Dedicated - Cz Republic
IQVIA UK
Prague, Czech Republic
On-site
Good clinical practice
Ich guidelines
Site selection and monitoring
IQVIA UK is seeking an experienced Clinical Research Associate to work on-site in Prague, Czech Republic. The role involves conducting site visits, ensuring compliance with regulatory standards, and collaborating with study site experts, requiring strong organizational and communication skills
Job Summary
Performing site selection, initiation, monitoring and close-out visits.
Evaluating the quality and integrity of site practices in accordance with regulatory requirements.
Collaborating with experts at study sites and with client representatives.
Matching Summary
Match Score: 85
IQVIA UK is seeking an experienced Clinical Research Associate to work on-site in Prague, Czech Republic. The role involves conducting site visits, ensuring compliance with regulatory standards, and collaborating with study site experts, requiring strong organizational and communication skills.
Skills & Requirements
Must-have
Good Clinical Practice
ICH guidelines
site selection and monitoring
subject recruitment planning
regulatory submissions tracking
Nice-to-have
flexible work schedules
career growth resources
therapeutic knowledge building
excellent working environment
Key Requirements
University degree in scientific discipline or health care
At least 2 years of experience as a Clinical Research Associate