Sr. Research Nurse (Department of Neurosurgery)

The Department of Neurosurgery is seeking a Sr. Research Nurse who will support the clinical and research activities of the Pain Institute, including NIH, non-profit, and commercially sponsored clinical trials. This role is hybrid in that the candidate will also play a role in the clinical care of our patient population. The Sr. Research Nurse will assist the principal investigators in the implementation of novel high-profile clinical trials across the department of neurosurgery. The successful applicant will be passionate about patient well-being, and improving the long-term trajectory for those patients through research and clinical care. The clinical role includes support of operations in

operating room, infusion, and clinic areas. While the nurse will work with a multidisciplinary team including physicians, research nurses, and research coordinators, applicants must be able to work and make decisions independently and have good time management skills in order to work on several projects simultaneously, and meet deadlines. Also, excellent organizational skills and data management are required, as well as flexibility and a willingness to help out members of the collaborative team, when such an occasion arises.

Specific Duties & Responsibilities.

• Screen potential participants for participation in trials and recruitment for studies through patient registries and relevant clinics.
• Ensure the informed consent process for studies, and coordinate participant enrollment and follow-up visits related to each respective study.
• The research nurse will also help with the collection of study data and biospecimens, entering data into study database, as well as documenting and reporting adverse events.
• Guide the activities of research coordinators or research assistants also working on those research projects on which this Sr. Research Nurse is working.
• Supervision of computer data entry, compilation and timely submission of summary reports, accurate record keeping of all study participant data, enrollment of study participants, appointments of study participants, monitoring of clinic visits and hospitalizations of study participants, chart review, home visits, specimen collection/processing, interviews and study subject follow ups.
• Assure Coordinator compliance with University and Division daily work policies and procedures.
• Reinforcing and promoting research staff compliance with Johns Hopkins human subjects research and good clinical practice policies.
• Coordination of study documentation (printing/filing/ copying/scanning for transmission of sponsors or collaborators).
• Reporting protocol deviations and adverse events in a timely manner.
• Will assist with the management of protocol related health problems, and maintain communication with members of the research team in a confidential manner and in accordance with good clinical practice.
• Interact with Study sponsors to initiate clinical studies, including IRB submission/management, budget development with CRSS (or internal), interface with ORA regarding contracts.
• External contact with members of the research study sponsoring agency, independent research monitors and ancillary center staff.
• Daily decision making regarding organizational aspects and logistics of study protocols.
• Hire and train new research coordinators that may join division on research administration, ethics, logistics and be responsible for their success.

Other research responsibilities include:

• Maintaining research related documents and correspondence in a confidential manner, including informed consent forms and research data.
• Resolving queries and reviewing monitoring reports to identify and correct errors.
• Maintaining study inventory according to regulatory standards.
• Reviewing with PIs research accounts status.
• Working with Compliance committees and Institutional Review Boards.
• Interacting with research subjects by email, phone, and in-person in a professional manner.
• Meeting with the research team on a regular basis, and participating in troubleshooting and resolving issues for research studies.

Specific Clinical duties and responsibilities include:

• Work with Medical Office Coordinators to relay provider input regarding medical decision making for patient inquiries for one provider.
• Communicates, consults and collaborates with other units/departments to assist in the comprehensive care of patients.
• Provides crisis intervention as needed, and triages complex cases; practices case management to ensure longitudinal care for patients, and coordinates scheduling of complicated patient treatment courses.
• Participates in ensuring a smooth operational clinic flow. Identifies barriers to service and creates solutions to ensure timely, safe, patient-centered care.

• Individual must be a registered nurse, licensed in the State of Maryland or state where practicing
• Bachelor's Degree in Nursing or related discipline.
• Two years experience in the specialty or a related area required.
• Additional experience may substitute for bachelor's degree and related master's degree may be considered in lieu of experience.

• Two years of clinical or research nursing experience in neurologic diseases is desired; Parkinson’s disease, memory disorders, or geriatrics experience desired, but not necessary.
• Master's Degree.

Current American Heart Association or American Red Cross CPR certification required.

Must maintain current licensure and certification during duration of employment.

Classified Title: Sr. Research Nurse

Role/Level/Range: ACRP/04/MF

Starting Salary Range: $76,980 - $134,995 Annually ($105,985 targeted; Commensurate w/exp.)

Employee group: Full Time

Schedule: M-F 8:30-5

FLSA Status: Exempt

Location: Hybrid/School of Medicine Campus

Department name: NUS Pain Institute

Personnel area: School of Medicine