Clinical assessment, treatment, and/or referral of participants who participate in the study
Participate in the routine assessment of participants in accordance with the protocols
Initiate, maintain, and strengthen referral systems via direct interaction and assist in the establishment of Memorandums of understanding (MOUs) as required by the study protocol/s
Conduct regular liaison with the laboratory regarding the interpretation of diagnostic test results. It is the responsibility of the clinician to ensure that an appropriate management plan is followed as a result of receiving diagnostic test results
Management of Hepatitis B vaccinations of Research center staff and maintaining accurate records
Screen and enroll eligible patients in accordance with the study protocol and ethical guidelines
Review patient vitals and other study-related results
Treat opportunistic infections diagnosed
Prescribe the appropriate treatment
Report any adverse events and follow up on patients
Provide regular clinical support to the clinic staff to ensure that clinical management of participants is of high quality and complies with HPCSA and WITS RHI standards
Data collection and storage of data according to GCP and study SOPs
Recruitment and retention according to set accrual targets as required by the sponsors
Development and ongoing revision of standard operating procedures compliant with sponsor and unit guidelines
Identify research questions in a specialist area
Write grant proposals, protocols, and ethics applications in order to fund and perform research studies
Implement research studies in conjunction with the research teams
Attend, present, and participate in organizational research and academic meetings
Produce monthly progress reports that document the clinical outcomes of study participants
Complete source notes and patient logs
Capture patient data on the Case Report Forms
Attend meetings as required
Engage and meet with sponsors and monitors as required
Attend to all staffing requirements and administration
Supervise and manage the duties of subordinates to ensure optimal staff utilization and maintenance of sound labor relations
Perform and facilitate performance development and assessments
Identify substandard performance by team members and take necessary corrective action
Coach and train subordinates and team members to ensure the acquisition of knowledge and skills required by the organization
Promote harmony, teamwork, and sharing of information
Take ownership and accountability for tasks and demonstrate effective self-management
Follow through to ensure that quality and productivity standards of own work are consistently and accurately maintained
Maintain a positive attitude and respond openly to feedback
Take ownership of driving your own career development by participating in ongoing training and development. activities such as workshops, forums, conferences, etc.
Participate and give input in ad hoc projects and initiatives
Comply with Good Clinical Practice (GCP), Protocol requirements, and Standard Operating Procedures (SOPs)
Verify the accuracy of data in source documentation and accuracy of transcription from source data Case Report Forms (CRF) as needed
Ensure errors on source documents e.g. CRFs are corrected, initialed, and dated
Support the timely transmission/data faxing of relevant Case Report Forms following QC activity (as needed)
Ensure completion of corrective action of internal and external QC reports and monitoring reviews
Assist with staff training (and retraining) where error trends are identified
Proactively resolve protocol queries and missing data with the Research Team
Required minimum education and training:
MBBCh Degree or equivalent
Required minimum work experience:
Minimum 3 years experience of which 1 should be in a research environment
Professional Body Registration:
Health Professions Council of South Africa (HPCSA)
Desirable additional education, work experience, and personal abilities:
Experience working in a donor-funded organization
Postgraduate qualification in Public Health/HIV management or in the process of obtaining the qualification
Experience in Reproductive Health
Experience in writing donor proposals, protocols, and scientific journals
Certification in HIV Management and good clinical practice
Well-organized, ordered, systematic, and analytical
Working knowledge of Microsoft Office
Assertive, confident, and adaptable
Able to work under pressure and adhere to deadlines
Self-motivated, able to work independently and work as part of a multidisciplinary team
Display concern for patients and willingness to respond to patients' needs and requirements
Able to prioritize own workload, take initiative (pro-active), and work to tight deadlines
Self-motivated with high regard for work ethic, values, and integrity
TO APPLY:
Only if you do meet the minimum job requirements and experience as mentioned above, you may submit a detailed updated CV.
Please Apply Online.
Please take note that the applicants who do not adhere to the above criteria will not be considered for the respective position.
The closing date for all applications: 12 January 2024.
Note AJ Personnel is fully POPI compliant.
Note WHC, in accordance with their Employment Equity goals and plan, will give preference to suitable applicants from designated groups as defined in the Employment Equity Act 55 of 1998 and subsequent amendments thereto.
Please note:
AJ PERSONNEL is only responsible for the advertising of the advertisement on behalf of their client Wits Health Consortium.
Wits Health Consortium will only respond to shortlisted candidates.
Candidates who have not been contacted within two weeks of the closing date can consider their applications to be unsuccessful.
AJ Personnel does not have any salary or other information regarding the position.
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