{"id":62725,"date":"2021-04-08T08:50:28","date_gmt":"2021-04-08T06:50:28","guid":{"rendered":"https:\/\/joblistsouthafrica.com\/?p=62725"},"modified":"2021-04-08T18:16:02","modified_gmt":"2021-04-08T16:16:02","slug":"aurum-group-current-job-recruitment-apply-now","status":"publish","type":"post","link":"https:\/\/joblistsouthafrica.com\/aurum-group-current-job-recruitment-apply-now.html","title":{"rendered":"Aurum Group Current Job Recruitment – Apply Now!"},"content":{"rendered":"
The Aurum Institute is offering a great opportunity to suitably qualified and experienced staff to contribute towards our mission to improve the health of people and communities through innovation in Health Research and Systems. We are focused on research, support and implementing integrated approaches to managing TB and HIV. The following positions have become available as part of the various projects currently being run by us and you are welcome to apply should you meet the requirements of the position.<\/p>\n
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Job Title: Research Assistants<\/strong> Job Summary:<\/strong> Research related activities:<\/strong> You will also be required to retain participants by;<\/strong> Work Experience:<\/strong> Minimum requirements:<\/strong>
\nLocation:<\/strong> Johannesburg, Gauteng, South Africa
\nReference #:<\/strong> Opt4TPTREF003
\nContract Type:<\/strong> Permanent
\nSalary:<\/strong> Market Related<\/p>\n
\nParticipant recruitment and enrolment
\nRecruit potential participants for the study
\nEnsure that potential participants are provided with all the study details as described in the Participant Information Sheet.
\nAdminister written informed consent
\nRecruit and schedule appointments for qualitative study participants
\nAssist study coordinator to plan recruitment schedules
\nConducting enrolment activities<\/p>\n
\nBeing responsible for the proper documentation of all study activities
\nAdminister data collection instruments as required.
\nCollect adherence data from electronic data monitoring devices
\nTranscribe qualitative interviews sessions
\nPerform quality checks on collected data.
\nData query resolution
\nComplete any other activities as required by the protocol or the study.
\nComplete, compile and submit study case report forms (CRFs) and source documents timeously
\nEnsure all records on participants are completed and accurately filed with strict adherence to documentation handling procedures
\nMaintain accurate study logs related to enrolment and other study activities.
\nReport on daily\/weekly activities to the Study Coordinator and meet stipulated enrolment and follow-up targets
\nParticipant retention<\/p>\n
\nObtaining, verifying and updating detailed locator data from participant for all visits.
\nIf possible, reminding participants about their appointments just prior to each visit
\nFollowing-up on participants to ensure study completion
\nRecommending retention strategies to study management
\nGeneral administration
\nYou will be required to;
\nPrepare participant files and documents.
\nReconcile reimbursement of participants
\nSafe storage and transportation of complete study documents
\nAttend study meetings to report on study progress
\nRequirements
\nKnowledge of:
\nMicrosoft Office
\nResearch methods
\nGCP training<\/p>\n
\nExperience in research at least 3 years
\nExperience in collecting qualitative and quantitative data
\nExperiencing in data entry and transcription
\nExperience working with staff in public healthcare facilities is advantageous<\/p>\n
\nQualification
\nGrade 12
\nPost-Matric Qualification
\nAdvantageous Requirements
\nWillingness to travel
\nDriver\u2019s license and driving experience
\nSkills required
\nGood communication skills.
\nAbility to solve practical problems.
\nGood management and interpersonal skills.
\nProficient in written and spoken English and fluency in local languages.
\nAbility to work independently and in a team. Ability to work under pressure
\nGood numerical skills<\/p>\n