×
Register Here to Apply for Jobs or Post Jobs. X

Clinical Research Nurse - Human Nutrition Research Center Aging

Job in Boston, Suffolk County, Massachusetts, 02298, USA
Listing for: Tufts University
Full Time position
Listed on 2026-06-13
Job specializations:
  • Research/Development
  • Healthcare
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Clinical Research Nurse - Human Nutrition Research Center on Aging

Overview

The mission of the Jean Mayer USDA-Human Nutrition Research Center on Aging (HNRCA) at Tufts is to promote healthy aging through nutrition science to empower people seeking to enjoy long, active, and independent lives. The HNRCA is one of the largest research centers in the world studying nutrition and its relationship to healthy aging and physical activity. We are one of six centers supported by the USDA.

The HNRCA investigators conduct some of the world's most advanced studies on nutrition and aging, making significant contributions to U.S. and international nutritional and physical activity recommendations, public policy, and clinical healthcare.

Clinical Research Nurses at the HNRCA are part of The Metabolic Research Unit (MRU). The MRU is one of the six Scientific Core Units at the HNRCA directed toward facilitating and supporting the clinical aspects of data collection with human study participants for the HNRCA's research teams. Clinical Research Nurses and support staff implement research protocols and continually assess and monitor study participants.

In addition to nursing services, the MRU is comprised of participant recruitment and enrollment, nutrition services from our metabolic kitchen, and study coordination services.

This is a grant funded position and is not eligible for severance pay.

What You'll Do

The Clinical Research Nurse is a registered professional nurse who manages the clinical course of research participants throughout a study. The primary function of the research nurse is to conduct human research protocols in a carefully monitored, controlled, yet dynamic environment to achieve quality outcomes for data and research participant safety to support the HNRCA research goals. The Clinical Research Nurse is responsible for knowledge of Code of Federal Regulations and Good Clinical Practice, policies and procedures of the Tufts Medical Center/Tufts University Health Sciences Institutional Review Board, and all other guidance documents for the conduct of human clinical trials and human research participant protection.

The Clinical Research Nurse utilizes the nursing process—assessment, planning, implementation, evaluation, and documentation—to attain research participant safety and data integrity.

  • Responsible for assessing prospective research participants for study eligibility and conducting review of research participant health history for multiple studies.
  • Admits research participants and obtains informed consents in accordance with procedures approved by the Tufts Medical Center/Tufts University Health Sciences Institutional Review Board.
  • Responsible for reviewing HNRCA/Tufts and USDA building regulations and federal regulations governing conduct on federal property.
  • Collaborates with multidisciplinary research team to coordinate study screening and enrollment; protocol treatment and follow-up care as needed.
  • Assesses changes in health and eligibility status throughout conduct of studies.
  • Recognizes, documents and reports medical issues, abnormal laboratory values, and adverse events to study MD/PI and tracks follow-up.
  • Delivers professional nursing care.
  • Conducts herself in a competent and compassionate manner.
  • Initiates medical emergency system as needed.
  • Responsible for accurate and complete documentation (written and electronic) in the research record for nursing‑related data for each protocol.
  • Follows HNRCA best practices for data collection, data retention and data QC procedures.
  • Implements, coordinates and monitors the safe and accurate collection of protocol‑specific clinical data on the MRU and occasionally offsite; documents and maintains all assigned study‑related procedures, processes and events.
  • Utilizes and implements the use of computer technology to increase efficiency, improve data integrity and implement quality assurance measures during data collection and documentation.
  • Develops, revises/updates data collection procedures and forms based on regulations and guidance documents; determines and secures equipment and supplies (to include pharmaceuticals).
  • Implements regulatory requirements required by the Tufts Medical Center/Tufts University Health Sciences…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)
0
200
Filters
Education Level
Experience Level (years)
Posted in last:
Salary