Research Nurse Specialist

Weill Cornell Medical CollegeNew York, NY
38d

About The Position

The Research Nurse Specialist performs a variety of technical and administrative duties concerning specific clinical research studies.

Requirements

  • Bachelor's Degree in Nursing
  • Approximately 2 years of related work experience in a clinical setting.
  • Strong verbal, written communications, and interpersonal skills.
  • Current NY State Registered Nurse License & Registration.
  • BLS certification, issued by the American Heart Association.
  • Infection Control Certificate

Responsibilities

  • Ensures optimal quality of medical care for patients participating in study; uses ethical conduct as established for healthcare personnel; assists in formation of educational aides and manuals as reference framework for patients and staff as necessary.
  • Participate in continuing education programs.
  • Educate nursing staff to drug protocols.
  • Assist with updating policies/procedures.
  • Keep abreast of new methods of treatment including the various venous access devices in the field.
  • Ensures optimal quality of medical care for patients participating in study; uses ethical conduct as established for healthcare personnel; assists in formation of educational aides and manuals as reference framework for patients and staff as necessary.
  • Arrange follow-up visits with patient to assess optimal quality of care and applies appropriate physical and psychological assessment to determine any effect of study drug.
  • Implement appropriate intervention in the event of adverse patient response.
  • Assess patient eligibility for inclusion in investigational studies.
  • Review patient history and abstracts and records information; records pre-study lab data; secure baseline laboratory blood work from patient and arrange necessary scans.
  • Review "informed consent" with patient; coordinate and educate patient and medical personnel as to required follow-up tests to be performed; assist physician in preparing IRB documents and maintain correspondence with sponsoring company/agency and IRB.
  • Assure adherence to study requirements according to protocol; monitor study drug according to protocol; monitor and/or perform pharmokinetic studies as detailed in protocol and attend to laboratory procedures to process, store and ship specimens.
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