Senior Clinical Research Coordinator

Want to run FDA IDE device trials hands-on, in a physician practice, instead of a big hospital research department? 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 Wilmington, DE site, an easy commute from Newark DE, West Chester, Media, Kennett Square, Elkton and South Jersey, and a reverse commute from Philadelphia. 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 South Jersey when studies need it. What you’ll do Screen, consent and enroll patients into device trials (ICH-GCP) Coordinate study visits, procedures and follow-up within protocol windows 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 Senior CRCs will also Lead studies from site start-up through close-out Train and support newer coordinators across the network Act as the main point of contact for sponsors and CRAs Help shape site processes as the network grows What you’ll bring CRC: 2+ years as a Clinical Research Coordinator Senior CRC: 4+ years as a coordinator, running device studies independently IDE or medical device trial experience (required for both levels) Working knowledge of ICH-GCP and FDA regulations Confidence working directly with physicians and patients Organized, reliable and comfortable working independently 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 Base $55,000–$85,000 depending on level and experience Per-patient enrollment bonus + yearly bonus potential #J-18808-Ljbffr Pragmatic