
Clinical research professional and social worker with over eight years of experience in clinical trials and public health research, specializing in HIV, TB, and mental health. Expertise includes clinical research coordination, participant recruitment and retention, informed consent processes, stakeholder engagement, and qualitative research. GCP-certified with formal training in research ethics, demonstrating strong skills in SOP implementation, data quality assurance using CRFs and REDCap, and regulatory compliance with HREC and POPIA standards. Currently advancing knowledge through a Master of Social Work at UCT, with a focus on mental health research and support for vulnerable populations.
Worked on Multiple Studies: Clinical Trials & Research Projects (HIV, TB, Implementation Science)
Providing HCT services to the community
Educating the community about HIV,TB and
sexual reproductive health
Distributing IEC material to the community
Strengething linkage to care
Creating demand for HIV testing in the community
Collaborating with community based organizations
Providing health care and counseling services to mine workers;
Psychosocial counseling
Crisis intervention
Conducting behavioral assessments
Case work and group work
Report writing
Stake holder engagement
Community Engagement
Awareness Campaigns
Adherence Counseling
Conducting employee wellness events
Formulating Case management Plans
Ensuring referral of client cases, management and following up
Assisting with the management of incapacity/disability cases
Clinical Trial Coordination
Good Clinical Practice (GCP)
Understanding of ethical research practices
Informed Consent & Participant Welfare
SOP Development & Implementation
Data Quality Assurance (CRFs, REDCap)
Regulatory Compliance (POPIA)
Participant Recruitment & Retention
Stakeholder Engagement
Qualitative research methodologies
Program evaluation
Project coordination
Supervising and developing teams
Psychosocial support