Clinical Research Coordinator 2

What you’d do

Coordinates moderate-risk clinical research studies, including screening and recruiting participants, performing study procedures and data collection, processing and shipping specimens, and documenting adverse events and protocol deviations. Full time. Found on the employer's careers page on Oct 17, 2026. Apply through the link.

You’ll need

• Bachelor's degree in relevant field
• Minimum 2 years of relevant experience
• Specimen collection, processing, and shipping
• Adverse event and protocol deviation documentation
• Learning agility and teamwork