Conduct clinical trials/studies according to ICH GCP, local regulations, study-specific protocols and NRC-specific processes
Perform clinical activities related to the trial protocol including clinical assessments, specimen collection, determination of clinical eligibility, and meticulous administration of study participant files.
Conduct clinical interviews and administer study questionnaires.
Completion of all required study-related documentation according to the study protocol, SOP and GCP requirements.
Conduct regular quality control checks to ensure accuracy of clinical data collection and good data quality.
Training of new nurses and capacitation of the clinical research team.
Clinical Trials Research experience essential : 1 to 2 years
Recognised nursing qualification
Valid registration with the South African Nursing Council
Previous experience in Clinical Trials Research
A valid ICH GCP certificate
Knowledge of HIV/AIDS and TB essential
Primary Health Care certification and NIMART training will be advantageous
Strong interest in clinical research and community development
Good communication and organizational skills within a multi-disciplinary team
Ability to multi-task and work under pressure.
IT proficiency and good knowledge in using Microsoft Office
Good administration skills, passionate about quality, detailed and meticulous in clinical record keeping
Must be able to work effectively as part of a team and as a leader
Valid Driver’s License
Fluent in English, Northern Sotho and Zulu
In order to apply for this job, please register your profile or log in with an existing account.