Clinical Research Coordinator Sr.

What you’d do

Oversees day-to-day clinical trial activities from startup to closeout, including screening, enrolling and consenting participants, data and specimen management, monitoring visit prep, and IRB documents. Full time; also trains and supervises research staff and helps develop workflows and SOPs. Found on the employer's careers page on Oct 8, 2026. Apply through the link.

You’ll need

• Bachelor's degree and 2 years clinical research experience, or Master's and 1 year, or HS diploma wi
• SoCRA certification (for the high school diploma path)
• Good Clinical Research Practice (GCP) knowledge
• Clinical trial coordination from startup to closeout
• IRB and regulatory document preparation