About this role

Responsible for the site management, site monitoring and close-out of assigned clinical trials
Ensure patient safety and quality study execution
Manage investigator site relationships for effective delivery of clinical trials
Safeguard the quality of investigator sites, including patient safety and compliance with GCP
Resolution of all protocol-related issues for assigned investigator sites
Work closely with the Site Care Partner, and other members of the study team

Minimum 1 year relevant experience in clinical research site monitoring and management
Knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience preferred
Must be fluent in English and in the native language(s) of the country they will work in
Valid driver’s license and passport required
Demonstrated knowledge of clinical research and development processes
Ability to work in a matrix team environment
Effective verbal and written communication skills

Clinical Research Associate / Senior Clinical Research Associate

Key skills