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Clinical Trials Nurse Specialist

2 weeks ago

Pretoria, Gauteng, South Africa Aj Personnel Full time

Responsibilities

  1. Ensure that screening, consenting, and enrollment of participants take place in line with project protocols.
  2. Verify that all participants have signed informed consent forms and maintain accurate records.
  3. Conduct study-related duties as specified by protocol, including phlebotomy and collecting study specimens.
  4. Maintain source document files, including logbooks, tracking logs, and reimbursement files.
  5. Record vital signs and observations for each participant during study visits.
  6. Assess and recognize respiratory illnesses in participants.
  7. Compile study progress reports and enter data into the required system on a daily basis.
  8. Track lost-to-follow-up participants and conduct home visits as needed.
  9. Educate participants regarding project aims and information.
  10. Complete source documentation at the time of participant visits and verify accuracy.