Clinical Research Coordinator
Medix
Responsibilities Looking for a mid-level to Sr. Coordinator that will oversee recruitment, screening, enrollment, scheduling, data collection, participant tracking, and invoicing. They will also be responsible for study start-up, budget negotiation, IRB submissions, modifications, and amendments, annual renewals, obtaining financial disclosure information from the investigators, preparation for audits and monitor visits, study closeouts Required Skills 2+ years experience as a Clinical Research Coordinator Strong understanding of Good Clinical Practice (GCP) and research regulations. Excellent communication and organizational skills, with the ability to manage competing priorities. Must be comfortable working directly with patients and handling biological samples. Must have a valid driver’s license and reliable transportation for required sample transport. Preferred Skills Experience in Rheumatology research ACRP or SOCRA certified Schedule/Shift 9am-6pm, M-F
Vacancy posted 2 days ago
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