John Mutisya

I am a clinical research professional with extensive experience conducting and monitoring clinical trials, from site initiation through close-out. I focus on ensuring regulatory compliance and data integrity across diverse study types.

At my current role with KEMRI-Wellcome Trust I contributed to protocol development, created risk-based monitoring tools, and prepared study materials including informed consent forms and CRFs. I have verified protocol and regulatory compliance across multiple studies such as Shigella and RSV trials.

Previously I coordinated program delivery for the Sydney Child Health Program at the local site, supporting participant enrollment, tutorials, and case report write-ups, and served as a Pediatric Clinical Officer overseeing clinical practice quality, staff scheduling, and monitoring visit execution.

I hold a Bachelor in Clinical Medicine and multiple professional certifications in clinical trial operations, GCP, adaptive trial design, risk-based monitoring, and data protection. I am committed to advancing medical care through rigorous clinical research and continuous quality improvement.