Perfect Malope
Driver’s License: Code 10 (C1)
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About
I am a strategic and dedicated research professional with progressive experience in quality assurance, research coordination, and compliance within clinical and social research environments. During the 8 years with The Aurum Health Institute I honed skills in research design, data analysis, quality systems oversight, internal auditing, stakeholder engagement, and reporting. I have proven ability to ensure research integrity, drive continuous improvement, and support the effective planning and implementation of research initiatives.
I bring a solid academic foundation in Gender Studies and Development Studies along with key clinical research certifications that support both qualitative and quantitative research competencies. My Core strengths include research management, audit and quality assurance leadership, data interpretation for policy‑relevant insights, team coordination, and stakeholder collaboration in all critical to supporting strategic research programmes and evidence‑based decision‑making.
Experience
Quality Assurance Officer - The Aurum Institute - Pretoria, South Africa
(2022 - 2025)
- Implemented and maintained quality assurance standards aligned with ICH‑GCP, South African regulatory requirements, and institutional SOPs.
- Led internal audits and supported external regulatory inspections with a strong focus on compliance and risk mitigation.
- Analysed quality data trends, identified risks, and recommended improvements to strengthen research operations and systems.
- Developed and supervised Corrective and Preventive Action (CAPA) plans to ensure quality improvements were institutionalised.
- Directed documentation control systems, ensuring accurate version control, compliance, and accessibility for research teams.
- Engaged effectively with multidisciplinary research teams and stakeholders to promote quality and operational transparency.
Research Assistant - The Aurum Institute - Rustenburg, South Africa
(2017 - 2022)
- Supported the execution of complex clinical research studies, facilitating participant coordination and high‑quality data collection.
- Ensured strict adherence to study protocols, ethical standards, and regulatory requirements throughout study lifecycles.
- Maintained complete, accurate regulatory documentation and ensured readiness for monitoring visits.
- Performed rigorous data verification and quality control checks to preserve data integrity and support reliable reporting.
- Collaborated with research staff, site teams, and stakeholders to facilitate smooth study operations and effective communication.
Education
Honours Degree - Gender Studies - University of Venda (2016 - 2017)
Bachelor of Arts - Development Studies - University of Venda (2013 - 2015)

