Sr. Clinical Research Coordinator- Endocrinology & Metabolism

What you’d do

Oversees day-to-day clinical trial activities per Good Clinical Practice, including IRB submissions, staff training, quality control, and data management. Full time. Found on the employer's careers page on Oct 19, 2026. Apply through the link.

You’ll need

• SoCRA certification with HS diploma and 6 years clinical research experience, or
• Bachelor's degree and 2 years clinical research experience, or
• Master's degree and 1 year clinical research experience
• Good Clinical Practice (GCP) knowledge
• IRB submission experience