Clinical Research Coordinator- PKPD (Evening Shift

What you’d do

Oversees day-to-day clinical trial activities under Good Clinical Practice, including data entry, query and inventory management, biospecimen processing and storage, shipments, and maintaining trial documentation. Full time, evening shift. Found on the employer's careers page on Oct 7, 2026. Apply through the link.

You’ll need

• High School Diploma or equivalent
• 4 years of relevant experience, or Bachelor's/Master's degree
• Good Clinical Research Practice (GCP) knowledge
• Clinical trial data entry and documentation
• Biospecimen processing and shipping