Wits VIDA Research Unit conducts cutting-edge scientific research
The Unit aims to save lives across Africa and, low and middle-income countries through translational research that informs local and global policy recommendations on infectious diseases and the use of next-generation and novel vaccines
Wits VIDA's research is focused on the clinical and molecular epidemiology of vaccine-preventable disease, clinical development and evaluation of vaccines, the study of the immunology of vaccines including in people living with HIV, and basic science research aimed at the discovery of potential vaccine epitopes
The Klebsiella II and GBS neurodevelopmental assessment projects are a component of the Pediatrics and Neonatal Surveillance (PNS) portfolio
This comprehensive portfolio encompasses viral and bacterial surveillance in infants and young children admitted to various hospitals
The studies within this portfolio delve into the origins and transmission of infectious diseases among different populations
Furthermore, they explore preventative and containment strategies to mitigate the spread of infectious diseases specifically in children
Main purpose of the job:
Responsible for coordinating all aspects of clinical research study activities and ensuring that clinical research projects are delivered and conducted smoothly and effectively
Location:
VIDA - Chris Hani Baragwanath Academic Hospital, Soweto, and the Rahima Moosa Mother and Child Hospital, Coronationville - Johannesburg
Key performance areas:Screening & Enrolment
Oversee study-specific patient recruitment, pre-screening, screening, and enrolment of eligible patients according to protocol requirements
Pro-actively identify and troubleshoot obstacles in the screening and pre-screening process
Conduct study-specific training as required
Oversee adequate study-specific files and record maintenance
Assist staff with study-related queries during screening and enrolment
Enforce procedures, policies, practices, and standards of the facility
Perform study-related procedures including but not limited to blood draws, vaginal and rectal swabs, and nasopharyngeal aspirates/swabs on infants and young children
Store swabs and blood samples and facilitate the transportation of samples to the VIDA laboratory
Carry out verbal interviews with the mothers or legally acceptable representatives of participants according to SOPs
Follow-ups & Research Administration
Oversee maintenance of adequate study-specific records including paper logs and electronic logs
Oversee management and printing of up-to-date versions of study source documents
Oversee retention of follow-up participants according to the study protocol, and pro-actively troubleshoot and identify areas of concern
Track study participants in-hospital as well as post-hospital discharge to ensure that all follow-up eligible participants attend the 1-year, 2-year, and 3-year face-to-face clinical visit
Maintain logs to remind study staff of the dates of follow-up of study participants
Liaise with the designated pediatricians to carry out follow-up neurodevelopmental assessment
Oversee relevant study stock management and ensure adequate stock levels are always maintained, and expired stock is sent for destruction timeously
Prepare daily and weekly statistics for the site
Present daily and weekly statistics to the principal investigator and senior study personnel as and when required
Data Quality Assurance & Control
Ensure all study activities are conducted according to a high standard of quality
Oversee resolution of any CRF, QC, and data queries
Oversee adequate and completeness of participant filing storage in collaboration with the QA team
Collaborate with the data manager to regularly monitoring and audit the database, including data verification, run data quality rules to check for duplicates, and ensure protocol adherence
Review reports on quality control findings, audit results, and corrective actions by the quality assurance team
Staff Management
Ensure that necessary performance management of all employees is done timeously. i.e., Probationary appraisals, one-on-ones, performance reviews, etc.
Attend to all staffing requirements and administration i.e. time sheets, leave forms, etc.
Supervise and manage the duties of subordinates daily by being involved on the floor
Identifying staff training needs and being involved with addressing these needs under senior supervision
Assist the team with ad hoc assignments and duties
Mentor, coach, and facilitate personal and professional staff development where possible
Effective Self-Management & Performance Ownership
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
Customer Service
Act in a professional and friendly manner in all dealings with internal and external stakeholders
Always show a high level of customer-centricity
Build and maintain authentic relationships with all stakeholders ensuring that all interactions are professional
Required minimum education and training:
Professional Nurse or equivalent Degree in Health Science related field
A valid GCP Certificate is advantageous
SANC or HPCSA registration
Required minimum work experience:
3 years of work experience with 2 years of research environment experience and 1 year of experience coordinating research studies
Desirable additional education, work experience, and personal abilities:
Clinical research experience
Excellent clinical skills
Driver's license
Computer literacy in MS Word and Excel
Good interpersonal skills
Ability to work in a team
Attention to detail
Motivated
Organized
Friendly
Professional
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: 23 May 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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