To ensure the integrity, compliance, and accuracy of research activities and data
To oversee adherence to regulatory standards, ensure data integrity, and implement quality control measures by Good Clinical Practice
Location:
Wits Vaccines & Infectious Diseases Analytics (VIDA) Research Unit - Chris Hani Baragwanath Academic Hospital, Soweto - Johannesburg
Key performance areas:
Quality assurance and control
Data review
Daily review of the RedCap Enrolment Log to ensure that all fields are correctly captured i.e., Hospital no; study ID; and enrolment criteria and status (eligible; enrolled)
Receive Lab Requisition Forms from RAs to check that all identifiers are correctly captured and crosscheck that the PET and hospital numbers are correct on the enrolment log
Review the data captured in the enrolment Log and PNS Database, storage, and retrieval processes of patient files to maintain data integrity and security, while adhering to data privacy regulations and GCP
Monitoring and Auditing
Conduct regular monitoring and auditing of the PNS Database, including data verification, run data quality rules to check for duplicates and ensure protocol adherence
Data Validation
Implement data validation procedures to verify the completeness, and reliability of the PNS data, preventing errors or data inaccuracies
Continuous Improvement
Implement quality improvement measures based on data analysis and feedback to enhance the reliability and efficiency of research processes
Collaboration
Communicate with all relevant departments (such as but not limited to the laboratory and field or clinical teams) to ensure study productivity, appropriate and effective problem-solving, and efficiency
Reporting
Prepare and submit reports on quality control findings, audit results, and corrective actions to the data and project manager
Administration
Organize and maintain study documentation, including informed consent forms, participant files, and sample log
Collect patient files from the clinical team from their office once a week
Verify patient file labeling in the filing room
Manage documentation related to quality assurance, including maintaining and organizing records, ensuring version control, and making documents accessible to authorized personnel
Maintain comprehensive records of quality assurance activities, audit reports, corrective actions, and compliance documentation
Establish procedures for accurate and comprehensive documentation of the lab requisition form and patient files to maintain transparency and traceability
Customer Service
Ensure all customer interaction (Both internal and external customers) is of the highest professional level
Build and maintain authentic relationships with all stakeholders ensuring that all interactions are professional
Effective self-management, and 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 own career development by participating in ongoing training and development activities
Required minimum education and training:
Matric/Grade 12
Good Clinical Practice (GCP) Certification
REDCap training is essential
Required minimum work experience:
2 years experience in a research environment
Minimum 1-year quality assurance experience in a research environment
Experience in electronic data capturing
Desirable additional education, work experience, and personal abilities:
Good verbal and written communication skills Basic computer literacy
High-level problem-solving ability needed
Exceptional self-management
Conscientious work ethic
Above-average attention to detail required
Motivated, organized, systematic and professional
Should be able to work under pressure with efficient multitasking
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: 02 February 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.
Apply
Company Description
The Vaccines and Infectious Diseases Analytics (VIDA) Research Unit of the University of the Witwatersrand, formerly RMPRU (Respiratory and Meningeal Pathogens Research Unit) has for over 20 years conducted numerous studies to assess the burden of and prevent vaccine-preventable diseases (VPD).