Clinical Research Coordinator - Endocrine Office

What you’d do

Coordinates multiple industry-sponsored and investigator-initiated clinical trials, from study start-up through closeout. Involves patient recruitment, eligibility screening, scheduling, physical assessments, biospecimen collection and processing, and data collection. Full time. Found on the employer's careers page on Oct 20, 2026. Apply through the link.

You’ll need

• Practical Nurse training (for LPN) or 2 years clinical/research experience
• Bachelor's degree or higher may substitute for 1 year experience
• Clinical trial coordination and study start-up experience
• Patient recruitment, screening, and biospecimen collection
• Full-time schedule