Oncology Clinical Research Coordinator 240245 Job at Medix™, Saint Louis, MO

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  • Medix™
  • Saint Louis, MO

Job Description

Responsibilities:

  • Knowledge of disease process, standard or care, and oncologic terminology
  • Knowledge of study protocol, inclusion and exclusion criteria and amendment training, study endpoints, reportable events (Adverse Event, Serious Adverse Event, Adverse Events of Special Interest)
  • Define methods of subject identification and recruitment
  • Weekly review of study visits completed, Electronic Data Capture (EDC) entries
  • Weekly review of study status
  • Conduct subject recruitment and confirm subject eligibility
  • Assists in recruitment efforts, contacting and identifying potentially eligible participants to screen
  • Coordinate study presentation and Informed Consent Form process with Co-Investigator; obtain consents for amendments where applicable
  • Scheduling and completion of all protocol required study visits and procedures
  • Preparation and maintenance of source documents and review with investigator
  • Maintain Investigational Product dispensing and accountability
  • Review Adverse Events and Serious Adverse Event with Primary Investigator within 24 hour of event report to Institutional Review Board (IRB) and sponsor.
  • Subject retention activities and follow up procedures
  • Protocol monitoring activities, preparation, data clarification
  • Coordination of assessment by investigator of patient, lab results and procedure findings to ensure safe and appropriate enrollment in study and prior to all treatments
  • Vital sign assessments, conduction of ECG, specimen collections, phlebotomy, IV and port insertion, treatment and removal, injections
  • Initiating chemotherapy infusions, maintenance and monitoring of infusion, and observation post infusion
  • Additional duties as assigned

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