Research Nurse

2 days ago

Boston, Massachusetts, United States Massachusetts General Hospital Full time
Job Summary

We are seeking a highly skilled and experienced Research Nurse to join our team at Massachusetts General Hospital. The successful candidate will be responsible for assisting in the implementation of Cardiology research protocols, working closely with the study team, and ensuring the smooth conduct of the study.

Key Responsibilities
  • Recruit and screen eligible patients for study participation, collect and compile case report forms, and coordinate related patient care activities.
  • Work with physicians, nurses, and patients to screen for study participation, obtain informed consent forms, and enroll patients into the study.
  • Coordinate and implement the research study according to the study protocol, including blood sample collection and processing.
  • Deliver professional nursing care, evaluate patients' responses to study protocols, and provide consultation to primary physicians and nurses.
  • Collaborate with the Principal Investigator regarding progress of the study and ensure the continuation or termination of study subjects according to the study protocol.
  • Act as liaison between patients and other members of the team regarding patient care activities related to the research protocol.
  • Submit clinical orders in Epic for research-related encounters per study protocol.
  • Conduct follow-up visits with patients as needed and perform physicals with patients.
  • Ensure clinical notes are well documented in EPIC when required.
  • Assist with the compilation of relevant patients' medical records from external hospitals/care centers.
  • Manage study documentation, schedule, and prepare for monitoring visits, close out the study appropriately.
  • Responsible for adverse event monitoring and reporting, document reportable events, and disseminate information to the PI, Study Monitor, and IRB as appropriate.
  • Act as liaison with study sponsor, study monitor, and Partners legal, budget, research management teams, and any other department involved in the study.
  • Prepare and submit protocols and protocol-related regulatory documents to the Institutional Review Board (IRB) and work with the IRB on an ongoing basis throughout the study.
  • Assist the PI in implementing site monitoring plans and responsible for study-site start-up and teaching.
  • Order equipment/supplies and use Epic to manage research-related billing, including enrolling patients in the study, linking orders, and reviewing charges per the contract and budget.
  • Invoice the sponsor for contract-required items using OnCore or an appropriate mechanism.
Requirements
  • Ability to forge productive working relationships with patients, families, staff, and co-workers.
  • Understanding of clinical research methodology and regulations is essential, with experience in clinical trial coordination, study monitoring, and project management required.
  • Leadership skills, good presentation and writing skills, and the ability to lead, interact well with others, take initiative, and think independently.
  • Excellent communication and organization skills, with attention to detail essential.
  • Cardiology knowledge is preferred, and knowledge of hospital systems and competency in MS Office programs, such as Word, Excel, and Outlook.
Qualifications
  • 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 - 2 years prior nursing experience; Minimum of - 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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