Clinical Research Coordinator - 249921

Present clinical trial concepts, study objectives, and treatment details to potential participants for cellular therapy trials; conduct comprehensive screening and assessments to determine eligibility. Participate in the informed consent process and enroll eligible patients in accordance with study protocols. Collect, maintain, and organize regulatory documentation in compliance with Standard Operating Procedures and applicable regulatory requirements. Coordinate and support monitoring and audit visits, serving as a point of contact for onsite monitors and auditors. Coordinate patient care activities to ensure adherence to protocol-specific requirements. Collaborate closely with physicians to monitor patients for changes in clinical status, adverse events, concomitant medications, protocol compliance, and treatment response, ensuring thorough and accurate documentation. Work directly with research sites, sponsors, and other study stakeholders to support trial operations. Oversee the preparation of physician orders to ensure ongoing protocol compliance. Communicate with physicians regarding study requirements, dose modifications, and adverse event reporting. Required Qualifications: At least two (2) years of experience in a clinical research setting Proficiency in essential clinical skills, including phlebotomy and obtaining vital signs Preferred Qualifications: Graduate of an accredited nursing program (BSN preferred) Minimum of one (1) year of nursing experience Current Registered Nurse (RN) licensure in the state of Virginia preferred #J-18808-Ljbffr Medix™