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, oversight of the safety of study participants, determination of clinical eligibility, and meticulous administration of study participant files.
Possibly conduct clinical interviews and administer study questionnaires.
Reporting, follow up, assessment and management of adverse events.
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 clinicians and nurses and capacitation of the research team.
Report writing and contribute towards publications.
Willing to rotate and provide back-up where required.
Coordinates relevant aspects of study and ensures compliance with study protocol, all relevant procedures, policies and regulations.
clinical research experience : 2 to 3 years
mbchb : 2 to 3 years
hpcsa : 2 to 3 years
ICH GCP Certificate : 2 to 3 years
MBChB degree with at least 2 year experience as a Medical Officer
Valid HPCSA registration as a Medical Practitioner, plus MPS membership
Previous experience in Clinical Research as a Principal Investigator or Sub-Investigator is preferred
A valid ICH GCP certificate
Exceptional general medical practitioner diagnosis and treatment proficiency
Knowledge of HIV/AIDS, TB, COVID-19 and Primary Health Care issues and ARV treatment 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 and other sponsor related programs and portals
Good administration skills, passionate about quality and detail and meticulous in clinic record keeping
Must be able to work effectively as part of a team and as a leader
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