To recruit, screen and provide health care to patients participating in clinical trials according to study protocols
Location:
King DinuZulu Hospital Complex - Durban, KwaZulu-Natal
Key performance areas:
Clinical assessment, treatment and/or referral of participants who participate in the study
Participate in 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
Quality control of case report forms with respect to clinical activities
Screen and enrol eligible patients in accordance with study protocol and ethical guidelines
Review patient vital statistics and other study-related results
Treat opportunistic or sexually transmitted infections diagnosed
Prescribe the appropriate treatment
Report any adverse events and follow-up on patients
Conduct ward rounds to follow up on patients who have been admitted to the hospital
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
Set up and maintenance of trial documentation required by regulatory authorities (Wits HREC )
Development and ongoing revision of standard operating procedures compliant with sponsor and unit guidelines
Ensure the maintenance of the study essential documents as per the Wits RHI/study SOP
Provide regular clinical support to the clinic staff to ensure that clinical management of participants is of a high quality and complies with HPCSA and Wits RHI standards
Identify research questions in 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 organisational research and academic meetings
Produce monthly progress reports which document recruitment and retention activities including study outcomes
Proactively resolve protocol queries and missing data with the Research Team
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 utilisation and maintenance of sound labour 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 organisation
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 for driving 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
Required minimum education and training:
MBBCh Degree or equivalent
Registration with Health Professions Council of South Africa (HPCSA)
Required minimum work experience and abilities:
Minimum 3 years of which 1 should be in a research environment
Experience working with trial participants, including provision of medical products by infusion, contraceptives, HIV/STI prevention and treatment services
Desirable additional education, work experience and personal abilities:
HIV management Certification
Post graduate Degree/Diploma in Public Health/Epidemiology or progress to this degree an advantage
Post graduate diploma (or training) in Obstetrics and Gynecology and Emergency medicine is an added advantage
Experience in providing sexual reproductive health especially managing STIs, providing contraception, taking pap smears, obtaining genital specimens such as cervico vaginal lavages and colposcopy examination is highly desirable
Experience working in a donor funded organization/NGO or project-based environment
Experience writing protocols and scientific journal articles
Exceptional organizational, administrative skills, with ability to work under pressure, adhere to tight deadlines and with a high regard for work ethic, values and integrity
Self-motivated, able to work independently and as part of a multidisciplinary team
Display a concern for patients and willingness to respond to patients needs and requirements
Working knowledge of Microsoft Office packages
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: 28 June 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.