
Website Wits Health Consortium
Job Description:
To provide support of clinical trials or clinical programs.
Job Responsibilities:
- Inform participants about the study.
- Collect Specimen as per study protocols (including informed consent process).
- Set up sample collection appointments.
- Ensure that all study projects are set up according to Good Clinical Practise (GCP).
- Screen potential participants and obtain informed consent according to SOPs.
- Record and maintain study documentation, including screening, enrolment, and withdrawal logs on daily basis.
- Collect participant data from medical notes and from the participants and complete CRFs (paper and electronic).
- Manage participant re-imbursements.
- Administer study questionnaires and or interviews.
Job Requirements:
- Must be customer /participant orientated
- Good communication skill
- Must be able to multitask
- Good filing skills
- Basic computer skills. Microsoft Word, Excel and Outlook
- Completion of Good Clinical Practice (GCP) courses will be advantageous
Qualification & Experience:
- Diploma in General Nursing
- Registration with the South African Nursing Council (SANC)
- Minimum 2-3 years nursing experience in clinical trials
Job Details:
Company: Wits Health Consortium
Vacancy Type: Full Time
Job Functions: N/A
Job Location: Parktown, Gauteng, SA
Application Deadline: N/A
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