Peter Nyamthimba Email & Phone Number

Kisumu, Kenya

• Expert in coordination of Mortality studies. Highly experienced in establishing and mentoring of teams that consent for autopsies in Mortality studies.Coordinating recruitment of study participants, screening of study participants, and enrolment of study participants.• Involved in community training and engagement on research participation • Seeking project approval, renewals and Communication with the Ethics Committees.• Hiring, Training, Supervision and Performance Appraisal of Project staff • Writing reports and documentation on study progress.• Effectively managed study data collection using an electronic data capture system • Excellently presented study progress and findings at local and international conferences.

Nairobi, Kenya

• Enhance production planning and inventory management and perform activities associated with monitoring clinical research studies, including phase I-III clinical trials as well as observational and epidemiology studies.• Spearhead the development of a study-specific monitoring plan, annotated CRFs, monitoring conventions, tracking forms, and other study-related documents as required.• Propel effective evaluation, development, set-up, training, and monitoring of client investigational sites participating in clinical trials for exceptional services.• Performs activities associated with monitoring clinical research studies, including phase I-III clinical trials as well as observational and epidemiology studies.• Create efficiency and smooth research management by pioneering the budgets and contracts negotiations, site selection and development.• Complete monitoring visits to review clinical data for accuracy, completeness and discrepancy resolution following the project plan.• Ensure SAEs, safety update reports and other new information or sponsor reports are provided to and received by the sites for reporting to ethics, as needed to improve compliance.

Western Kenya

Kisumu, Kenya

• Ensuring that research studies are implemented according to the protocol.• Supervising and coordinating research projects, including protocol development, ethical approvals, training, data collection, analysis, report writing, presentations, and manuscript development.• Closely collaborate with other key stakeholders in the department to develop and manage project timelines and budgets.• Facilitating training, motivating, supervising and capacity building of staff• community education and engagement to strengthen research acceptance.

Masters, Project Planning And Management

Certificate, Clinical Research Associate

Diploma, Healthcare Management

Certificate, Clinical Trials Management

Certificate, Clinical Research

Certificate, Health Communication

Certificate, Clinical Research