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 Nurse<\/strong> Job Summary:<\/strong> Research study-related tasks:<\/strong> Administrative:<\/strong> Managerial Tasks:<\/strong> Other responsibilities:<\/strong> Qualifications:<\/strong> Attributes:<\/strong> Skills required:<\/strong> Experience:<\/strong> Please note:<\/strong>
\nLocation:<\/strong> Klerksdorp, South Africa
\nReference #:<\/strong> 2021\/06\/03\/01 6 Months<\/p>\n
\nClinical tasks:<\/strong>
\n\u2022 Conduct clinical research activities in the day-to-day implementation of research studies at Aurum\u2019s site, ensuring the accurate, timely,
\ncomplete, ethical and efficient processing of study volunteers in accordance with the study protocol.
\n\u2022Take medical histories and conduct physical examinations, including pelvic, genital and rectal examinations
\n\u2022Collect and store blood and other specimens
\n\u2022Perform urine, rapid HIV, and pregnancy testing
\n\u2022Syndromic management of STIs
\n\u2022Dispense medication for STIs and Family Planning
\n\u2022Educate, counsel and\/or refer study participants for care related to HIV\/AIDS, STIs, Family Planning, medical circumcision and TB
\n\u2022Assist with HIV and Risk Reduction counselling
\n\u2022Perform basic clinical procedures on screening volunteers and study participants as trained\/required. These could include:
\n\u2022measuring and recording vital signs,
\n\u2022Assist with participant education, counselling and consenting process
\n\u2022Ensure smooth completion of participants visits<\/p>\n
\n\u2022Assist with procedures related to the recruitment and screening of potential study participants
\n\u2022Assist with assessing and recording the eligibility \/ ineligibility of potential study participants
\n\u2022Conduct procedures related to the enrolment of study participants that are eligible
\n\u2022Assist with the conduct of procedures related to the tracing, retention and follow-up of study participants
\n\u2022Complete, compile and submit study case report forms (CRFs) and source documentation timeously
\n\u2022Administer research data collection instruments
\n\u2022Respond timeously, accurately, and in keeping with GCP to data queries from the QA and Data Management team
\n\u2022Respond timeously, accurately, and in keeping with GCP to data queries from the Lab team(s)
\n\u2022Respond timeously, accurately, and in keeping with GCP to data queries from external vendors
\n\u2022Monitor and report on the safety of trial participants<\/p>\n
\n\u2022Process and store study documents with strict adherence to documentation handling procedures.
\n\u2022Ensure procurement, stock control and disposal of clinical supplies in compliance with regulatory standards.
\n\u2022Implement blood and urine specimen processing and shipping procedures
\n\u2022Maintain accurate study logs related to biological specimens
\n\u2022Assist with keeping stock of clinic supplies
\n\u2022In adherence to relevant SOPs and GCP standards, document all clinical tasks as required and ensure that records are filed correctly and timeously
\n\u2022Respond timeously to data queries from the QA and Data Management teams
\n\u2022Provide study administrative assistance as needed, including but not limited to data entry, filing, printing of specimen labels, etc.<\/p>\n
\n\u2022Assist with staff recruitment and orientation
\n\u2022Conduct supervision, quality control, and corrective training of junior clinical staff<\/p>\n
\n\u2022Conducts all activities listed above according to SOPs and protocols, and in accordance with confidentiality agreements.
\n\u2022Ensures the ethical, timely, accurate, confidential and courteous processing of research participants and data
\n\u2022Conducts other duties as reasonably assigned
\nRequirements<\/p>\n
\n\u2022Registered Professional\/Enrolled Nurse \/ Enrolled Nursing Assistant with the HPCSA
\n\u2022Dispensing License<\/p>\n
\n\u2022Ethical
\n\u2022Results driven
\n\u2022Emotional intelligence
\n\u2022Business acumen
\n\u2022Analytical thinking
\n\u2022Self starter<\/p>\n
\n\u2022Attention to detail
\n\u2022Leadership skills
\n\u2022Management skills
\n\u2022Interpersonal skills<\/p>\n
\n\u2022Experience in clinical research and\/or HIV\/AIDS-related work
\n\u2022Computer literate
\n\u2022Valid GCP certificate
\n\u2022Good phlebotomy and pelvic examination skills
\n\u2022Experienced in contraceptive counselling
\n\u2022Experienced in STI syndromic management
\n\u2022Independent, detail-oriented, results-driven individual
\n\u2022Good interpersonal & communication skills, with demonstrated ability to work in inter-disciplinary teams and with diverse staff and clients
\n\u2022Valid driver\u2019s licence and own transport<\/p>\n
\nKindly provide current and relevant references for background checks
\nAll appointments are subject to the preferred candidates obtaining the necessary security clearance, reference checking and competency assessment. We embrace employment equity and are committed to achievement of fair and equal representation of our workforce. Preference will be given to internal applicants and candidates from previously disadvantaged backgrounds.
\nAurum welcomes applications from all persons with disabilities
\nWhilst 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