Clinical Research Coordinator - Full-time

Want to run FDA IDE device trials hands-on, in a physician practice, without the commute into the city? Our client, a fast-growing clinical research network, runs FDA-regulated IDE and post-market medical device trials with leading vascular and endovascular practices. They're hiring a Clinical Research Coordinator or Senior Clinical Research Coordinator based at their West Orange, NJ site, a short commute from Montclair, Livingston, Maplewood, Morristown and most of Essex, Morris and Bergen counties. You'll be the research lead at the site: working directly with the physicians, owning your studies day to day, and growing with a network that's expanding fast. Occasional travel to nearby sites in New Jersey when studies need it. Apply or message me for a confidential conversation and the full details. Coordinate study visits, procedures and follow-up within protocol windows Keep regulatory binders audit-ready Enter data and resolve queries in EDC systems Prepare for and host sponsor monitoring visits Be the go-to contact for physicians, clinic staff and sponsors Lead studies from site start-up through close-out Train and support newer coordinators across the network Help shape site processes as the network grows CRC: 2+ years as a Clinical Research Coordinator IDE or medical device trial experience (required for both levels) Hands-on IDE trials in vascular and endovascular medicine ~ Real ownership of your site and studies ~ Clear path from CRC to Senior CRC as the network grows ~ Per-patient enrollment bonus ~