Cedar Health Research is seeking a Data Specialist to ensure data accuracy, integrity, and timeliness from study startup through closeout. You will support data collection, review, and cleaning in line with GCP, ICH, FDA and sponsor requirements.
Collaboration with PIs, CRCs, regulatory staff, monitors, sponsors, and CROs is essential. Qualified candidates have 2–5 years of clinical data management, hands-on EDC experience (Medidata/Oracle/Veeva/RealTime), and strong attention to detail.
#J-18808-LjbffrRemote Clinical Trials Data Specialist in dallas at Unknown Company
This position is listed as full time and onsite.