Senior Clinical Research Coordinator

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.What you'll doScreen, consent and enroll patients into device trials (ICH-GCP)Coordinate study visits, procedures and follow-up within protocol windowsKeep regulatory binders audit-readyEnter data and resolve queries in EDC systemsPrepare for and host sponsor monitoring visitsBe the go-to contact for physicians, clinic staff and sponsorsSenior CRCs will alsoLead studies from site start-up through close-outTrain and support newer coordinators across the networkAct as the main point of contact for sponsors and CRAsHelp shape site processes as the network growsWhat you'll bringCRC: 2+ years as a Clinical Research CoordinatorSenior CRC: 4+ years as a coordinator, running device studies independentlyIDE or medical device trial experience (required for both levels)Working knowledge of ICH-GCP and FDA regulationsConfidence working directly with physicians and patientsOrganized, reliable and comfortable working independentlyWhy joinHands-on IDE trials in vascular and endovascular medicineReal ownership of your site and studiesClear path from CRC to Senior CRC as the network growsBase $55,000–$85,000 depending on level and experiencePer-patient enrollment bonus401(k) with company match