Study Coordinator at Kenya Medical Research Institute
1 month ago
Kenya Medical Research Institute (KEMRI) is a State Corporation established through the Science and Technology (Amendment) Act of 1979, which has since been amended to Science, Technology and Innovation Act 2013. The 1979 Act established KEMRI as a National body responsible for carrying out health research in Kenya.
Vacancy No. FN-02-02-2024
Duties and Responsibilities
Develop an in-depth understanding of the study protocols, goals and logistics required to conduct research studies and implementation projects
Develop clinical trial implementation plans in collaboration with investigators and relevant stakeholders
Create Standard Operating Procedures (SOPs) that align with the study protocols
Conduct training for research teams to always guarantee adherence to study SOPs at all times.
Provide leadership in research studies through coordination and daily oversight of day-to-day implementation of study activities
Coordinate the study team to ensure proper performance of study and project activities consistent with study protocols and SOPs
Lead study recruitment with the support of study investigators and research team, including evaluating potential participants for inclusion in clinical trials in compliance to the study protocol
Perform study visits and clinical assessments of study participants, document study procedures, and interpret laboratory results in collaboration with study PIs.
Ensure proper documentation of all research participants in physical and electronic medical records
Ensure participant safety through monitoring of clinical and laboratory adverse events
Ensure timely reporting of adverse events and protocol deviations.
Ensure participant privacy and confidentiality are maintained
Compiling weekly clinical and study data and study reports in coordination with data manager
Oversee and monitor study budget expenditure, including study resource utilization, cash flow and expenditures
Maintain relationships with collaborating partners and the County Ministry of Health
Coordinate communication with research staff and PI/Co-PIs/Co-Investigators
Maintain regular communication with members of the research team
Ensure regular and timely updates of clinical trial recruitment, follow-up, and data collection progress
Work professionally and ethically with competence, accountability, and integrity
Perform any other relevant duties as assigned by the study PIs
Requirements
Qualifications:
Bachelor of Medicine and Surgery
Be duly registered with the relevant professional body, holding valid practice license
Other Desirable Qualifications:
Knowledge in Cervical Cancer Screening and Prevention Clinical or research programs
Attention to detail, critical thinking and problem-solving skills
Interpersonal and communication skills
Good communication skills
Experience working in HIV care, either in a Clinical or Research setting
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Nairobi, Nairobi Area, Kenya Kenya Medical Research Institute - KEMRI Full timeKenya Medical Research Institute (KEMRI) is a State Corporation established through the Science and Technology (Amendment) Act of 1979, which has since been amended to Science, Technology and Innovation Act 2013. The 1979 Act established KEMRI as a National body responsible for carrying out health research in Kenya.Vacancy No. FN Duties and Responsibilities...
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Nairobi, Kenya Kenya Medical Research Institute - KEMRI Full timeKenya Medical Research Institute (KEMRI) is a State Corporation established through the Science and Technology (Amendment) Act of 1979, which has since been amended to Science, Technology and Innovation Act 2013. The 1979 Act established KEMRI as a National body responsible for carrying out health research in Kenya. Vacancy No. FN-02-02-2024 Duties and...
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