You agree that you have familiarised yourself with South Africa’s Protection of Personal Information Act and understand your rights and obligations under this Act. TASK may process your personal information for recruitment purposes for suitable posts that may arise within the organisation. Meeting our employment equity goals will be acknowledged during the recruitment processīy responding to this advert and sending your cv, cover letter and/or any other documentation, you are consenting to TASK processing your personal information as contained in the furnished documents. TASK reserves the right to withdraw this advertisement and not fill the above-mentioned vacancy at any stage during the recruitment process. Please send applications to you have not heard from us within one month, please consider your application as unsuccessful. Please indicate in your application that you are applying for the above-mentioned position. Flexibility to help out at other TASK sitesĪrea: Bellville, Brooklyn, Delft (Cape Town)Īpplications closing date: 9 September 2022.Practical experience in research and/or clinical trials would take preference.Computer and internet competency and basic knowledge of Microsoft Word, Excel, Outlook.Valid Nursing Council certificate (SANC).
Is competent to undertake resuscitation procedures
Is competent in professional registered nursing procedures including the following – vital signs, ECG measurements, phlebotomy, IV preparation, administration and monitoring, medication administration and control. Performs miscellaneous job-related duties as assigned. Ensures the site files are updated at all times with latest study documentation at study start, during the study and at study close out. Enters source data timeously and accurately into electronic or paper-based case report forms (CRFs). Administers IP as per protocol and keep the IP administration log up to date and verify storage are within allowed range as per protocol. Documents procedure actual times and results directly and accurately in source documents. Performs sputum collection (via sputum induction if needed) Collects and prepares study specimens and keeps accurate records for laboratory personnel. Familiarizes themselves with normal ranges in vital signs, ECG measurements, safety blood ranges, in order to identify abnormalities and act/document accordingly to ensure subject safety. Ensures subject safety, protocol compliance and prevent protocol deviations at all times. Reviews source documents for accuracy and completeness Completes source documents, logs and checklists accurately and in real time according to GCP specifications. Plans ahead and perform study specific procedures in a protocol-correct manner and within given timelines and in specified order, with the assistance of pre-drafted prompt sheets Documents patient care and procedures in pre-drafted source documents. Ensures optimal subject preparation, care and safety at all times for all subject visits. Assists the investigator in verifying whether all in- and exclusion criteria are met before randomization. Makes relevant appointments for study participants, liaises with City of Cape Town and provincial government clinic staff Assists lead study nurse/nursing manager with scheduling of study participants. Perform quality check on ICF (informed consent form) Assists the investigator in signing of the IC document and ensures that adequate time and privacy for reflection and answering questions has been provided. Educates, cares for and supports the study participants throughout the course of the trial Undertakes the informed consent (IC) process by presenting a study to possible participants and/or family members. Key Performance Areas (KPAs) & Responsibilities include, but not limited to: The RN ensures that the clinical trials are run according to protocol and Good Clinical Practice (GCP) requirements at all times ensuring all procedures are documented in source and data is accurately transcribed onto clinical research forms (CRF) or electronic-CRF’s. The RN will be responsible for specialized nursing activities such as phlebotomy, taking of vital signs, symptoms procedures, ECG measurement, administering oral and IV medications, injections, cannulation, and holistic patient care. 
The purpose of this role is to perform procedures following the visit schedule as stipulated in each protocol and monitor the health and safety of the participants, and document the response to an intervention, which is typically new drug or therapy in the source documents.
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