The School of Medicine, Department of Urology is accepting applications for a Research Nurse II position. In this role and under the guidance and supervision of the Principal Investigator, the Research Nurse Specialist II (RNS II) is responsible for assuring that the integrity and quality of the clinical research trial is maintained and that the trial is conducted in accordance with Good Clinical Practice Guidelines, federal and sponsor regulations and guidelines and Vanderbilt Policy and Procedure.
The RNS II plans and implements recruitment procedures for potential participants, manages enrollment of the trial from screening to randomization to study completion, ensures compliance with protocols and overall research and clinical objectives, manages study-related procedures as required by the protocol, maintains accurate and timely documentation and maintains communication with the sponsor.
In this role you will perform the following duties:
- The ability to work both independently and as a team is crucial.
- Administration of trial research and survey of patients.
- Review database for potential study participants
- Design/revise source documents
- Initiate or continue informed consent process
- Screen, enroll, and randomize study participants
- Schedule all f/u visits per study protocol
- Schedule numerous tests and procedures with multiple departments and physicians
- Make sure PI, Sub-I's, and other research personnel are compliant with study procedures and document and report deviations that do occur as required by sponsor and IRB
- Communicate with sponsors, CRO's, central labs, central pathology/radiology regarding study progress
- Attend investigator meetings
- Educate study subjects and other departmental personnel regarding study requirements
- Nursing care including but not limited to; phlebotomy, EKG's, VS, histories, injections, medication dispensing, PVR's, UA's, bladder instillations, etc.
- Package and ship lab specimens (in absence of Clinical Trials Associate)
- Maintain drug and lab supplies for assigned studies
- Source document completion
- Completion of CRF's - paper and electronic
- Resolve queries, assist in data locks, and interact with monitors
- Create and maintain databases for study protocols
- Prepare and submit IRB documents for annual review
Key Functions and Expected Performances:
- Knowledge and understanding of policies, procedures, and regulations governing human subject's research and incorporation of them in the conduct of research and care of participants
- Possesses a basic awareness of the Federal regulations governing the protection of human subjects, e.g., FDA, OHRP, GCP/ICH guidelines, and HIPAA regulations
- Proficiently prepares and processes new IRB research proposals, amendments, continuing review applications and adverse events according to institutional and departmental policies and procedures and federal regulations
- Possesses a basic awareness of the Vanderbilt policies and regulations governing the protection of human subjects
- Knowledge and understanding of the management and implementation of clinical trial operations
- Understanding and capability to perform the procedures required of each study protocol (obtains training needed to safely and accurately perform or assess required procedures)
- Prepares and stores critical documents required to be maintained and provided to the sponsor prior to, during and after the conduct of a clinical trial
- Performs packaging and ships study medication and specimens (blood, urine, etc.) to the sponsor or laboratory in accordance with IATA and sponsor shipping guidelines
- Participates in periodic site visits from sponsor, regulatory authorities and others to review research, source documentation and research procedures
- Participates in the determination of eligibility and recruits candidates for study participation. Troubleshoots trial recruitment strategies to ensure trials are completed in a timely manner through implementing effective screening and recruitment strategies and completing required documentation.
- Provides education and training to appropriate personnel and participants in research specific methodology and procedures
- Maintains open and positive communications with investigators, participants, co-workers, other departments and sponsors.
- Digests complex clinical information to determine if documentation is accurate, complete, and to ensure procedures contain appropriate safeguards. Ability to multi-task, managing multiple assignments while maintaining documentation and study visits and procedures in a timely manner.
- Understands standard of care versus research and continually assesses need for additional protections for the protection of research participants and the accuracy and appropriateness of research data.
- Utilizes nursing skills and processes to identify participant and study problems and utilizes problem solving skills to identify solutions, following through to implement solutions, and assuring goals are met.
- Proactively involved in quality improvement through ongoing assessment and through the identification of issues, and planning and evaluation of quality improvements.
- Serves as an advocate for human subjects by establishing and maintaining communication with Investigators, research staff, Sponsors, participants and representatives of professional organizations, participant advocates, and the public responsible for, or concerned about, protections for human participants of research
- Assesses and evaluates potential participants pertinent medical and historical information to ensure only appropriate subjects are enrolled in clinical trials
- Participates in the ongoing informed consent process, ensuring that human subjects, their families, and other health care providers clearly understand what is expected of and from them in the course of participating in a clinical trial
- Utilizes nursing skills to complete research protocols including patient recruitment, screening, scheduling and organizing of study visits, enrollment, assessments, interviews, laboratory and diagnostic studies, medication dispensing and other protocol specific investigational procedures
- Independently uses and documents the nursing process to plan, deliver and evaluate goal focused, individualized, safe, age-specific care as it relates to uncomplicated research participants and with assistance for complicated research participants
- Performs procedures for research as they are described in the protocol, deviating from the protocol only when a subject's safety is at risk and reports all deviations from the protocol to the Principal Investigator and/or senior personnel who will determine of a protocol amendment or other safety assessments are required
- Maintains accurate records to document recruitment efforts, telephone follow-up interviews and research data
- Utilizes knowledge of disease processes to observe for and report adverse events in a timely and accurate manner to the principal investigator and all regulatory authorities (IRB, Sponsor, FDA, NIH, etc.) as required by protocol, policies and procedures and regulations
- Conducts literature searches and assesses new information as appropriate regarding new studies and at the time of continuing review to keep up-to-date in the research field of study in order to determine if significant historical or new findings exist that may impact the risk/benefit ratio of the research participant
- Actively identifies and participates in training, education, and development activities to improve own knowledge and performance to sustain and enhance professional development. Pursues avenues to ensure awareness of the latest information available to nurses conducting clinical research, for example
- Reviews the Research Support Services website to obtain information regarding available and required in-services, required certifications and to obtain important updates
- Attends the Clinical Research Staff Council monthly meetings
- Attends in-services advertised by the Institutional Review Board, Research Support Services, professional societies, etc
- Demonstrates initiative in self-directed learning, as evidenced by attendance of professional development opportunities. Actively seeks new learning opportunities. Sees learning as part of work
- Assumes responsibility for continuous learning, engaging in a minimum of 10 hours of educational activities annually or pursuing an advanced academic education or certifications
- Develops and achieves personal and professional goals
Graduate of an accredited RN nursing program required; BSN preferred
1-2 years of RN experience or equivalent required
Prior Clinical Trial Experience
Prior experience with Urology is strongly preferred.
CCRC/CCRP certification is a plus
Experience working with sponsor-initiated trials preferred
Refined interpersonal skills and the ability to work independently
Strong interpersonal and leadership skills in dealing with healthcare providers and patients and their families
Strong organizational skills, creativity, ability to "think outside the box," and a positive attitude are vital
Licensure, Certification, and/or Registration (LCR):
- TN Registered Nurse
Job Research Nursing
Primary Location TN-Nashville-Medical Center North (MCN)
Organization Urology 104775