GRACIOUS CHILOANE

GCP-certified Pharmacology Honors graduate with hands-on research experience in protocol-driven studies, demonstrating a solid foundation in clinical documentation, research ethics, and data integrity. Proven ability to maintain accurate records while supporting compliance activities and coordinating essential research-related documentation. Eager to contribute skills and knowledge as an entry-level Clinical Trial Assistant or Clinical Research Assistant within a CRO, hospital, or research organization. Committed to advancing clinical research and ensuring the highest standards of quality and compliance.

RESEARCH EXPERIENCE

Honors Research Project – University of the Witwatersrand (2025) .

Detection, isolation, and characterisation of bacteriophages active against XDR Klebsiella pneumoniae .

• Participated in the planning and implementation of research data collection activities .
• Captured experimental and research data into structured datasets and ensured completeness .
• Performed data cleaning, verification, and organisation to maintain data quality.
• Assisted with basic statistical analysis and interpretation of research results .
• Compiled written research reports and summaries to address project and supervisory requirements .
• Prepared and presented research findings in written and oral formats .
• Adhered strictly to ethical, confidentiality, and data protection requirements.
• Developed strong laboratory competencies through honours-level research, including microbiological techniques, data recording, and adherence to biosafety and research protocols.