Nurse Research Project Manager

The Nurse Research Project Manager plays a key role in the administration and coordination of clinical research projects, supports the day-to-day conduct of clinical research and other sponsored projects while performing nursing responsibilities in accordance with protocol requirements. This position provides direct coordination of study visits, ensures regulatory and protocol compliance, manages study documentation, and delivers patient-centered clinical care to research participants. This position plays a key operational role within the department of medicine, assisting with studies from start-up through completion under the guidance of the PI and research leadership. Coordinates assigned clinical studies from initiation through close-out under PI direction Organizes study start-up activities, including feasibility, regulatory submissions, and staff scheduling. Prepares, maintains, and reconciles study documentation such as source notes, case report forms, and regulatory binders. Schedules and conducts participant visits; ensures accurate data capture and protocol adherence. Monitors participant safety, performs follow-up, and reports adverse events promptly. Serves as a liaison between investigators, clinical staff, sponsors, and ancillary departments (pharmacy, lab, imaging). Assists in IRB submissions, amendments, and continuing reviews. Maintains participant confidentiality and secure handling of study records. Serves as a liaison between investigators, clinical staff, sponsors, and ancillary departments (pharmacy, lab, imaging). Performs clinical duties per protocol, including biospecimen collection, study-drug administration, EKGs, and other nursing procedures within scope of practice. Provides patient education and informed-consent discussions in coordination with the PI. Collaborates with care teams to integrate study participation with standard clinical treatment. Advocates for participant safety and wellbeing throughout the research process.Education/Experience:Bachelor of Science in Nursing, requiredLicenses or certifications:RN-Registered Nurse - DORA - Department of Regulatory Agencies required.BLS-Basic Life Support (BLS/CPR) - AHA - American Heart Association or American Red Cross required.CITI trainingPrior experience:1-2 years of clinical research 2 (+) years of Clinical Bedside NursingCritical Care Experience PreferredKnowledge/Skills/AbilitiesAbility to manage project timelines and competing prioritiesFamiliarity with OMB Uniform Guidance and NIH grant policiesStrong communication and documentation skillsDetail-oriented and capable of navigating complex institutional processesProficiency in Microsoft Office SuiteKnowledge of IRB submission platforms and regulatory databasesPhysical demands:Frequent sitting for administrative workOccasional walking and standing in clinical areasOccasional lifting of study materials and files (under 20 lbs)Environmental demands:In Person office and clinical exposurePotential exposure to patient care settings and biological samplesUSD $109,200.00/Yr.USD $136,500.00/Yr.

Created: 2026-03-02