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Kisumu
Jacinta Badia

Jacinta Badia

Senior Clinical Researcher

Healthcare

Kisumu

Social

Services offered

I am a skilled Research Monitor, Senior Clinical Research Coordinator/QAQC Officer with considerable 9 years’ professional experience in research and an in-depth knowledge in managing successful delivery of clinical trials. Manages quality assurance/controls and the execution of clinical protocol and data management for a number of clinical trials at multiple sites, ensuring compliance with all regulatory and contractual requirements. Establishes and maintains sound clinical and data collection practices to ensure validity of studies. Monitors the conduct and progress of the studies to ensure compliance with established protocols, appropriate research methodology, and study timelines. Participates in protocol development, site selection, study initiation and termination activities. Develops and completes final study reports, maintain communication with regulatory authorities and take lead in development of CAPA plans and implement quality improvement activities. l have invaluable experience with budget management and monitoring, expenses control, managing project resource allocation, building the capacity of staff, community mobilization, manuscript writing, and analyzing qualitative and quantitative data. 

Research monitor
Qaqc officer
Clinical research coordinator
Approximate rate: KSh 2,000 per hour

Experience

I am a skilled Research Monitor, Senior Clinical Research Coordinator/QAQC Officer with considerable 9 years’ professional experience in research and an in-depth knowledge in managing successful delivery of clinical trials. Manages quality assurance/controls and the execution of clinical protocol and data management for a number of clinical trials at multiple sites, ensuring compliance with all regulatory and contractual requirements. Establishes and maintains sound clinical and data collection practices to ensure validity of studies. Monitors the conduct and progress of the studies to ensure compliance with established protocols, appropriate research methodology, and study timelines. Participates in protocol development, site selection, study initiation and termination activities. Develops and completes final study reports, maintain communication with regulatory authorities and take lead in development of CAPA plans and implement quality improvement activities. l have invaluable experience with budget management and monitoring, expenses control, managing project resource allocation, building the capacity of staff, community mobilization, manuscript writing, and analyzing qualitative and quantitative data. 

Education

Mastersin Public Health with basic diploma in Clinical Medicine

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