Join us as a Clinical Research Associate I or II to perform and coordinate clinical monitoring and site management processes across global clinical trials
Job Summary
Join us as a Clinical Research Associate I or II to perform and coordinate clinical monitoring and site management processes across global clinical trials.
You will ensure trials are conducted according to approved protocols, ICH-GCP guidelines, and applicable regulations while maintaining audit readiness and collaborative relationships with investigational sites.
The role involves frequent travel, exposure to clinical environments, and contributing to project teams for process improvement and communication facilitation.
Matching Summary
Join us as a Clinical Research Associate I or II to perform and coordinate clinical monitoring and site management processes across global clinical trials.
Skills & Requirements
Must-have
Risk-based monitoring approach
Protocol and regulatory compliance
Clinical trial documentation management
Root cause analysis and problem solving
Frequent travel to site locations
Good communication with medical personnel
Microsoft Office proficiency
Nice-to-have
Critical thinking skills
Team collaboration and independent work
Customer focus and listening skills
Process improvement initiatives
Adaptability in diverse scenarios
Key Requirements
Bachelor's degree in life sciences or Registered Nursing certification
1 to 2 years clinical monitoring experience for CRA I; over 2 years for CRA II