Job Title

Medix is hiring a Clinical Research Nurse to support oncology trials in Hartford, CT! This is a full time, on-site position with a Monday- Friday schedule. This is a great opportunity for RNs in Clinical Research or Oncology to work within a growing organization! Job Responsibilities:Coordinate and facilitate the appropriate conduct of clinical research trials in oncology 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 teractcollaborate with all physicians, other members of the health care team and participantsfamilies 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 screeningenrollment 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.Assistcoordinate preparation for internal and external audits.Handle all confidential information appropriately. Qualifications: Bachelor's degree NursingMinimum of 1 year of relevant clinical research experience or oncology experienceDemonstrated clinical competency with patient related measurements and with a high degree of accuracy with respect to documentation and data collection.Ability to work with spreadsheets (such as Excel), familiarity with databases and querying.Experience in preparing and completing Case Report Forms (CRF's), eligibility checklist and other relevant documentation protocols.Excellent interpersonal skills are required for working with the study participants and working as a member of a highly integrated team. Schedule: Monday- Friday 8am- 5pm On site in Hartford, CT Interviews are taking place now - Apply today!