Clinical Research Nurse

19 hours ago


Chelsea, Massachusetts, United States Mass General Brigham Full time
Job Title: Clinical Research Nurse

Mass General Brigham is seeking a highly skilled Clinical Research Nurse to join our team. As a Clinical Research Nurse, you will play a critical role in the implementation of cardiology research protocols, working closely with the study team, including study physicians, study monitor, and Cardiology administration.

Key Responsibilities:
  • Identify and recruit eligible patients, collect, compile, and complete case report forms for the study sponsor and coordinate related patient care activities in the inpatient and outpatient setting.
  • Work with physicians, NP/PAs, nurses, and patients to screen for study participation.
  • Obtain all necessary approvals and informed consent forms; screen and enroll patients into the study.
  • Coordinate and implement the research study according to the study protocol, including blood sample collection/phlebotomy and processing.
  • Using the nursing process delivers professional nursing care and evaluates patients' responses to study protocols, provides consultation to primary physicians, nurses, and technicians regarding protocol implementation and contributes to research publications.
  • Collaborate with the Principal Investigator (PI) regarding progress of the study, and the continuation/termination of study subjects according to study protocol.
  • Acts as liaison between patient and other members of the team regarding patient care activities relating to the research protocol.
  • Submits clinical orders in Epic for research-related encounters per study protocol.
  • Conducts follow-up visits with patients as needed, may perform physicals with patients.
  • Ensures clinical notes are well documented in EPIC when required.
  • Assist with the compilation of relevant patients' medical records from external hospitals/care centers.
  • Manages study documentation, schedule and prepare for monitoring visits, close out study appropriately.
  • Responsible for adverse event monitoring and reporting; documents reportable events and other major concerns related to the studies and disseminates the information to the PI, Study Monitor and IRB as appropriate.
  • Acts as liaison with study sponsor, study monitor and Partners legal, budget, research management teams and any other department involved in the study.
  • Prepares and submits protocols and protocol related regulatory documents to the Institutional Review Board (IRB); works with the IRB on an ongoing basis throughout the study.
  • Assists the PI in implementing site monitoring plans.
  • Responsible for study-site start-up and teaching.
  • Orders equipment/supplies.
  • Uses Epic to manage research-related billing including enrolling patients in the study in Epic, linking orders, and reviewing charges per the contract and budget.
  • Invoices sponsor for contract-required items using OnCore or appropriate mechanism.
Requirements:
  • RN from an accredited school of nursing and MA Licensure as an RN.
  • Bachelor of Science in Nursing preferred; new graduates must have a BSN degree.
  • Must have 1 – 2 years prior nursing experience; Minimum of 1 - 2 years research-related experience preferred.
Working Conditions:

Duties will be performed in a research office, the operating rooms, and other inpatient and outpatient settings.



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