Registered Nurse/ Clinical Research Coordinator

About the role

Peters Medical Research is seeking an initiative-taking, detail-oriented Registered Nurse / Clinical Research Coordinator (RN/CRC) to join our growing clinical research team. The RN/CRC will coordinate and conduct clinical research studies while providing nursing expertise and direct clinical support to research participants and the research team. This position combines traditional Clinical Research Coordinator responsibilities with direct patient care, clinical assessments, medication administration, laboratory procedures, and support of medically complex research visits. The RN/CRC will assist with assigned clinical trials from study startup through closeout and serve as a clinical resource to other research staff. The ideal candidate will possess excellent organizational and communication skills, strong clinical judgment within the nursing scope of practice, and a commitment to patient safety, research quality, and protocol compliance.

Responsibilities

• Coordinate and conduct assigned Phase I–IV clinical research studies in accordance with study protocols, GCP, IRB requirements, sponsor requirements, and site policies
• Conduct screening, enrollment, study visits, follow-up visits, and other protocol-required activities
• Review medical records and assist in assessing potential research participants against protocol inclusion/exclusion criteria
• Obtain and document medical histories, medications, vital signs, ECGs, laboratory results, and other clinical information
• Perform venipuncture, IV placement, blood collection, specimen processing, ECGs, and other protocol-required procedures within training and scope of practice
• Administer investigational products, infusions, injections, and protocol-required medications when appropriately delegated and permitted
• Monitor participants during dosing, infusions, and research procedures and promptly identify and escalate adverse events or changes in clinical status
• Assist Investigators with the assessment, documentation, and follow-up of adverse events and safety events
• Provide clinical support during medically complex and Phase I research visits, including PK visits and prolonged observation periods
• Complete accurate and timely source documentation and maintain complete research records
• Enter study data into EDC and other sponsor systems and resolve data queries within required timelines
• Assist with maintaining regulatory and