{"id":70293,"date":"2022-01-04T08:00:24","date_gmt":"2022-01-04T06:00:24","guid":{"rendered":"https:\/\/joblistsouthafrica.com\/?p=70293"},"modified":"2022-01-04T19:39:50","modified_gmt":"2022-01-04T17:39:50","slug":"aurum-group-recent-job-recruitment-apply-now-6","status":"publish","type":"post","link":"https:\/\/joblistsouthafrica.com\/aurum-group-recent-job-recruitment-apply-now-6.html","title":{"rendered":"Aurum Group Recent 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: Quality Officer – Klerksdorp <\/strong> Job Summary:<\/strong> Requirements:<\/strong> Other:<\/strong>
\nLocation:<\/strong> Klerksdorp, North West, South Africa
\nReference #:<\/strong> 2021\/11\/24\/04
\nContract Type:<\/strong> Permanent
\nSalary:<\/strong> Market Related<\/p>\n
\nYOUR JOB WILL BE:<\/strong>
\nConducting in-house monitoring to ensure compliance with ICH\/GCP, standards, Protocol and other Guidelines as applicable.
\nEnsure that all staff are using current versions of Study documents, e.g. Protocol specific documents, program specific documents.
\nData verification of source data and relevant documents e.g. CRF\u2019s, and other data collection forms.
\nGive ongoing feedback on type of findings\/trends etc.
\nIdentify training needs in, and give feedback to the relevant Study Coordinator\/Project Manager.
\nDeveloping and maintaining systems to ensure that correct data is collected by relevant staff
\nRaising study related queries with the Quality Manager, Principal Investigator, Project Manager and Study Coordinator to ensure clean and accurate data
\nReview project developed source documentation.
\nProvide training on quality related topics.
\nPrepare for monitoring visits
\nSOP\/WPG review and writing as applicable
\nReview corrective\/preventive actions
\nAssisting the Quality Manager in implementing the Quality Management Plan
\nPerforming other duties as delegated by the Quality Manager
\nEnsuring version control of study documents
\nEnsuring timely reporting of all project activities using predefined indicators
\nPerforming quality control of recording and reporting procedures including checking data collection tools for accuracy
\nApply national and International legislation(s) pertaining to research
\nAbility to generate reports from Excel Data
\nConducting QC1, QC2 and data verification activities<\/p>\n
\nYOU SHOULD HAVE:<\/strong>
\nRelevant degree\/diploma in Health, Sciences or Social Sciences or equivalent education
\nValid GCP certificate
\nWork Experience:
\nAt least 2 years clinical research experience
\nClinical or research experience
\nPrevious work experience in a quality assurance\/control environment advantageous
\nProficiency in written and spoken English<\/p>\n
\nValid Driver\u2019s license
\nOwn transport advantageous
\nAbility to work independently and in a team
\nOpen and clear communicator
\nFocused on quality and detail
\nWorking Knowledge of MS Packages
\nData Analysis Skills<\/p>\n