Clinical Research Project Manager

What you’d do

Manages multiple clinical research studies, preparing protocols, consent forms, recruitment and training materials, and IND applications. Acts as liaison with sponsors, the IRB, core labs, site PIs, and study staff, and coordinates trial start-up and patient recruitment. Full time. Found on the employer's careers page on Oct 19, 2026. Apply through the link.

You’ll need

• Clinical research study management experience
• Prepare study protocols and informed consent forms
• IND application preparation and submission
• Liaison with sponsors, IRB, and site PIs
• Trial start-up and patient recruitment coordination