AddressKenya Medical Research Institute, Off Mbagathi Way Nairobi
About Kenya Medical Research - KEMRI
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 r... read moreesearch in Kenya.
Key Responsibilities:
Greet and assist participants, visitors, and staff in a friendly and professional manner
Manage front desk operations, including answering phones, scheduling participant
Key Responsibilities:
Installing, inspecting and testing installations in the institute
Preparing repair and maintenance schedules in the relevant sections for institute infrastructure, instal
Key Responsibilities:
Ensure compliance with KEMRI policies, NACOSTI, SERU/IRB approvals, KPPB, and international research ethics standards.
Oversee contracts, sub-awards, MTAs, DTAs, and data
Key Responsibilities:
Assist in the selection of appropriate suppliers and contractors, to promote good procurement practice with due regard to sustainability, ethical purchasing standards and c
Key Responsibilities:
Assist in the development and implementation of standard operating procedures (SOPs) for all study procedures
Create training schedules for the study, track and create re
Key Responsibilities:
Carry out literature review and design and develop protocols to address the research objectives
Conduct study entry preparatory activities including obtaining all relevan
Key Responsibilities:
Carry out literature review and design and develop protocols to address the research objectives
Conduct study entry preparatory activities including obtaining all relevan
Key Responsibilities:
Design, develop, and update data entry forms and surveys using REDCap to ensure efficient and accurate data collection.
Implement branching logic, skip patterns, and vali
Key Responsibilities:
Plan, manage, and supervise the day-to-day operations of the study.
Supervise the study teams (Research Assistants and Data Analyst) to ensure that the study is conducted
Key Responsibilities:
Read and understand the study protocol, and develop, review, and ensure adherence to study standard operating procedures (SOPs) in line with protocol requirements
Develop
Key Responsibilities:
Develop, review and adhere to the study standard operating procedures (SOPs).
Sensitize the community/health facilities teams on the study- Provide health education on PM
Key Responsibilities:
Develop, review and adhere to the study standard operating procedures (SOPs)
Sensitize the community/health facilities teams on the study.
Respond to questions about th
Key Responsibilities:
Assessing patients and clients and establishing health care needs;
Planning and implementing care interventions based on patients’/clients’ health needs;
En
Key Responsibilities:
Ensure adherence to ICH-GCP, local regulations, and ethical standards.
Monitor compliance with study protocols, SOPs, and sponsor requirements.
Identify deviations, non
Key Responsibilities:
Dispense investigational products, compounded medicines, and concomitant medications per protocol and Standard Operating Procedures
Maintain accurate participant/patient
Key Responsibilities:
Receive, label, process, and store biological specimens in accordance with study protocols and Good Clinical Laboratory Practice (GCLP) standards.
Perform routine and spe
Key Responsibilities:
Prepare and manage sign-in sheets, appointment logs, and visit or records
Handle inquiries in person, via phone, or email, and direct them appropriately
Assist in print
Key Responsibilities:
Enter data from Case Report Forms (CRFs) into Electronic Data Capture (EDC) systems with high accuracy.
Perform source data verification and assist in resolving data disc
