Clinical Research Coordinator

Conduct patient visits in accordance with study protocols, performing clinical tasks such as vital signs, EKGs, specimen collection, and phlebotomy. Obtain and document informed consent while educating participants to ensure a positive experience. Monitor subject safety by reporting adverse events and escalating concerns as appropriate. Complete timely source documentation and EDC data entry, resolving queries to ensure data integrity. Maintain investigational product accountability and support monitoring visits, audits, and inspections. Collaborate with site staff and investigators to ensure protocol adherence and efficient visit flow. Requires 2+ years of clinical research experience and proficiency in EDC and CTMS applications.