About the role
Job Family: Nurse Travel Required: None Clearance Required: Ability to Obtain Public Trust What You Will Do: We are currently searching for a Research Nurse to support clinical research through participant coordination, data collection, and regulatory oversight. This is a full-time, on-site opportunity in Rockville, MD. Monitor integrity, completeness and timeliness of clinical data collection. Problem-solve complex or unpredictable situations and improve processes and services to patients and colleagues. Participate in clinical practice and research support meetings and develop multidisciplinary performance improvement programs and projects to improve operating procedures, patient care and decrease costs. Monitor activities pertaining to clinical protocols such as monitoring patient recruitment and retention, trial progress, and the need for extension or renewal of ongoing trials. Develop and maintain internal documents for clinical trials not supported by Clinical Research Organizations. Recruit, screen, consent, and coordinate participants for clinical research studies and trials. Conduct clinical assessments, collect medical histories, and support patient safety and clinical care activities. Ensure protocol compliance, human subjects protection, informed consent, and regulatory adherence. Review adverse event safety datasets, serious adverse events reports, external safety reports, and protocol deviations to ensure participant safety, data integrity and regulatory compliance. Manage IRB submissions, adverse event reporting, protocol amendments, deviations, annual reviews, and regulatory documentation. Oversee clinical trial operations, participant recruitment and retention, data collection, quality assurance, and study progress monitoring. Perform clinical data management, analysis, interpretation, and reporting to support research objectives and regulatory
requirements. Develop and maintain study documentation, standard operating procedures, and trial tracking systems. Collaborate with multidisciplinary research and clinical teams to improve processes, resolve complex issues, and enhance study performance. Train and mentor research staff, clinicians, and trainees on protocol implementation, regulatory