Clinical Research Nurse

2 weeks ago


Hartford CT United States Medix™ Full time

Responsibilities:

  • Coordinate and facilitate the appropriate conduct of clinical research trials in oncology which may be supported by the NCI, industry, cooperative groups or HHC system alliances.
  • Coordinate and conduct the operation of clinical trials as per GCP and ICH guidelines including participant recruitment; informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring.
  • Interact/collaborate with all physicians, other members of the health care team and participants/families across the system in a manner that supports the conduct of clinical trials.
  • Required to attend the respective system-wide Disease Management Team meetings and present the clinical trials to potential investigators.
  • Collaborate with and support other clinical trial staff across the system to ensure highest quality clinical research activities.
  • Document relevant data collections into various sponsor electronic data capture systems and complete data entry within protocol timelines.
  • Prepare study calendars and materials; maintain participant tracking logs and screening/enrollment logs.
  • Assist regulatory staff with study regulatory reporting requirements and IRB policies for protocol deviations, safety reporting and continuing reviews.
  • Assist research account specialist of CCRO with clinical trial billing in the resolution of related queries.
  • Assist/coordinate preparation for internal and external audits.
  • Handle all confidential information appropriately.


Qualifications

  • Bachelor’s degree Nursing
  • Minimum of 2-3 years of relevant clinical research experience.



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