Clinical Research Associate, Sponsor Dedicated

What you’d do

Monitor clinical trial sites, including selection, initiation, monitoring and close-out visits, and manage site relationships to keep studies compliant with protocol and regulations. Full time; must reside in the country where the job is located. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• Bachelor's in scientific discipline or health care preferred
• 2+ years independent on-site CRA monitoring experience
• CRO, sponsor, or similar setting experience
• Site monitoring visits per Good Clinical Practice
• Must reside in the country where the job is located