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2 months ago
We are seeking a highly skilled Clinical Research Nurse to join our team at the Jean Mayer USDA-Human Nutrition Research Center on Aging (HNRCA) at Tufts University. As a key member of our research team, you will play a critical role in conducting human research protocols in a carefully monitored, controlled, yet dynamic environment to achieve quality outcomes for data and research participant safety.
Key Responsibilities- Assess prospective research participants for study eligibility and conduct review of research participant health history for multiple studies.
- Admit research participants and obtain informed consents, execute intra-study informed consents for multiple studies in accordance with procedures approved by the Tufts Medical Center/Tufts University Health Sciences Institutional Review Board.
- Collaborate with multidisciplinary research team to coordinate study screening and enrollment, protocol treatment and follow-up care as needed.
- Assess changes in health and eligibility status throughout conduct of studies, recognize, document and report medical issues, abnormal laboratory values to study MD and track follow-up.
- Administer investigational substances according to protocol and regulatory requirements, use the following nursing skills for data collection: phlebotomy, IV (insertion and maintenance), volumetric infusion pump use, gastric tube placement and sampling, resting metabolic rates, EKG, assist with protocol procedures e.g. fat biopsy, muscle biopsy, etc.
- Assess protocol tolerance and compliance, collect and document participant health and research data, deliver professional nursing care, conduct self in a competent and compassionate manner.
- Inform PI/MD of pertinent clinical issues and adverse events, initiate medical emergency system as needed, responsible for accurate and complete record keeping for nursing-related data for each protocol.
- Follow HNRCA best practices for data collection, data retention and data QC procedures, implement, coordinate and monitor the safe and accurate collection of protocol-specific clinical data on the MRU and occasionally offsite.
- Graduate of an accredited nursing program.
- Active Massachusetts Registered Nursing (RN) license in good standing.
- IV and phlebotomy skills.
- Clinical nursing experience in a hospital, clinic, or similar health care setting.
- Proficient in Microsoft Office Word and Excel.
- Completion of Human Research Participant Protection training within 2 weeks of start date.
- CPR and AED certification within 2 weeks of start date.
- Experience in clinical research and working with research participants.
- Experience working within IRB guidance and policies.
- Experience with REDCap or other research data collection databases.
The schedule for this position is either Monday, Tuesday and Friday or Wednesday, Thursday and Friday.
Pay RangeMinimum $71,050.00, Midpoint $88,850.00, Maximum $106,700.00
