Registered Nurse

Duties/Pligte
- Conducting clinical research, including enrolling patients in research studies, implementing research protocol and presenting findings as required;
- Collecting and analysing data, including managing databases and record keeping;
- Reporting research findings, which may include presenting findings at conferences, meetings and other speaking engagements where applicable;
- Keeping record of all stock, equipment, and pre-packed laboratory kits;
- Reporting and documenting all missed visits on that same day;
- Complying with all regulatory requirements to ensure Good Clinical Practice (GCP);
- Complying with study procedures, FAMCRU SOP'S and GCP standards;
- Adhering to the Quality Assurance Plan implemented for the specific study;
- Reporting any congenital anomalies and clinical conditions to the sub-investigators;
- Completing source documentation as required by the study specific protocol;
- Engaging with internal and external stakeholders, including community groups as required i.e., MOU's, day hospitals, and hospitals;
- Assisting with the recruitment of participants for studies and providing direct patient care for participants.
- _
- Uitvoering van kliniese navorsing, met inbegrip van die inskrywing van pasiënte vir deelname aan navorsingstudies, implementering van navorsingsprotokol en

aanbieding van bevindings soos vereis;
- Versamel en ontleed data, met inbegrip van die bestuur van databasisse en rekordhouding;
- Rapporteer navorsingsbevindings, wat die aanbieding daarvanby konferensies, vergaderings en ander spreekbeurte kan insluit waar van toepassing;
- Rekordhouding van alle voorraad, toerusting en voorafverpakte laboratoriumstelle;
- Rapportering en dokumentasie van alle gemiste besoeke op dieselfde dag;
- Voldoening aan alle regulatoriese vereistes om Goeie Kliniese Praktyk (GKP) te verseker;
- Voldoening aan studieprosedures, FAMCRU SOP'S en GKP-standaarde;
- Voldoening aan die gehalteversekeringsplan wat vir die spesifieke studie geïmplementeer is;
- Rapportering van enige aangebore afwykings en kliniese toestande aan die sub-ondersoekers;
- Voltooiing van brondokumentasie soos deur die studie-spesifieke protokol vereis word;
- Skakeling met interne en eksterne belanghebbendes, met inbegrip van gemeenskapsgroepe soos vereis, dit wil sê: MOU's, daghospitale en hospitale;
- Hulpverlening met die werwing van deelnemers aan studies en verskaf direkte pasiëntsorg vir deelnemers.

Job Requirements/Pos Vereistes
- Diploma in General Nursing Science;
- Registered membership with the South African Nursing Council (SANC);
- Three years' clinical experience in a research environment;
- A good command of isiXhosa and / or Afrikaans;
- A valid driver's licence.
- _
- Diploma in Algemene Verpleegkundige;
- Geregistreerde lidmaatskap met die Suid-Afrikaanse Raad op Verpleging (SANC);
- Drie jaar se kliniese ervaring in 'n navorsingsomgewing;
- 'n Goeie begrip van isiXhosa en / of Afrikaans;
- 'n Geldige rybewys.

Recommendation/Aanbeveling
- Experience in conducting clinical research, including enrolling patients in research studies, implementing research protocol and presenting findings;
- Excellent attention to detail required in collecting and analysing data;
- Strong written and verbal communication skills for interacting with patients and reporting research findings.
- Valid GCP will be advantageous.
- Ervaring met kliniese navorsing, met inbegrip van die inskrywing van pasiënte in navorsingstudies, implementering van navorsingsprotokol en aanbieding van bevindings;
- Uitstekende aandag aan detail wat vereis word in die insameling en ontleding van data;
- Sterk skriftelike en mondelinge kommunikasievaardighede vir interaksie met pasiënte en verslagdoening van navorsingsbevindings;
- Geldige GKP sal voordelig wees.