{"id":70435,"date":"2022-01-10T08:50:38","date_gmt":"2022-01-10T06:50:38","guid":{"rendered":"https:\/\/joblistsouthafrica.com\/?p=70435"},"modified":"2022-01-10T16:51:56","modified_gmt":"2022-01-10T14:51:56","slug":"the-aurum-institute-current-job-opportunity-apply-now-6","status":"publish","type":"post","link":"https:\/\/joblistsouthafrica.com\/the-aurum-institute-current-job-opportunity-apply-now-6.html","title":{"rendered":"The Aurum Institute Current Job Opportunity – Apply Now!"},"content":{"rendered":"
The Aurum Institute is offering a great opportunity to suitably qualified and experienced person to contribute towards our mission to improve the health of people and communities we work in through innovation in Clinical Research. We are focused on preventative vaccine research for communicable diseases , including HIV, COVID and RSV with an expanding portfolio. The position below has become available at the Aurum Pretoria Research Site. You are welcome to apply should you meet the requirements of the position.<\/p>\n
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Job Title: Research Doctor (Principal Investigator)<\/strong> Job Summary:<\/strong> Technical Work Responsibilities:<\/strong> Requirements:<\/strong> Experience:<\/strong> Requirements:<\/strong> <\/p>\n Aurum welcomes applications from all persons with disabilities:<\/strong><\/p>\n Whilst all applications will be carefully considered, only short-listed applicants will be interviewed. If you do not hear from us within 21 days of the closing date, this will mean that your application has been unsuccessful. All interviewed applicants will receive feedback as part of our continued drive towards people development<\/p>\n
\nLocation:<\/strong> Pretoria, Gauteng, South Africa
\nReference #:<\/strong> 2022\/01\/04\/03
\nContract Type:<\/strong> Permanent
\nSalary:<\/strong> Market Related<\/p>\n
\nThe Research Doctor (Principal Investigator) takes overall responsibility for all aspects of the clinical trials assigned to them. This includes the accurate, timely, complete, ethical and efficient processing of study volunteers in accordance with the Study Protocol and procedure manual, and Good Clinical Practice.<\/p>\n
\nLiaise with Internal and External Stakeholders for the specific clinical trials
\nApply relevant clinical knowledge and skills within protocol guidance
\nApply knowledge and understanding of communicable diseases
\nOversee Research Study-related tasks, such as regulatory processes, recruitment and retention of participants, quality assurance processes, laboratory and pharmacy processes.
\nAttending and conducting training activities relevant to the specific clinical trial
\nReporting and record keeping relevant to the specific clinical trial
\nResearch-related administrative duties
\nPerformance management of staff conducting the specific clinical trial<\/p>\n
\nEducation:<\/strong>
\nBachelor\u2019s degree from college or university in Medicine
\nRegistered Medical Practitioner with the HPCSA
\nGCP Certification<\/p>\n
\nAt least 2 years\u2019 experience as a Principal Investigator of a Clinical Trial is mandatory
\nExtensive experience as a research clinician is required with Principal Investigator experience in a minimum of two clinical trials.<\/p>\n
\nProficient personal computer skills
\nProficient in written and spoken English and fluency in other local languages would be advantageous
\nSA Citizen or valid work permit to work in South Africa
\nValid Driver\u2019s License
\nWilling to work overtime when required.
\nMeticulous attention to detail and open to quality review of all work done<\/p>\n