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:
Design, execute, and optimize molecular biology, NGS, and bioinformatics experiments under the supervision of the Principal Investigator.
Analyze complex datasets from a
Key Responsibilities:
Supporting manuscript writing, editing, and submission for peer-reviewed journals.
Assisting with grant proposal development, including drafting concept notes, budgets, a
Key Responsibilities:
Timely extraction of data from patients’ charts
Verify quality of data by comparing abstracted data to source documents
Ensure facilities have adequate data colle
Key Responsibilities:
Clinical research data collection
Clinical management for cervical cancer prevention and women living with HIV
Support counseling as needed
Participate in screening,
Key Responsibilities:
Clean and sanitize clinic rooms, offices, restrooms, and common areas daily.
Dispose of waste and ensure proper segregation of recyclable and non-recyclable materials. Ma
Key Responsibilities:
Provide Tier 1–2 technical support (onsite/remote), manage the helpdesk queue, and document issues, resolutions, and SOPs.
Set up, secure, and maintain staff endpoi
Key Responsibilities:
Provide high-quality clinical care to participants, including HIV testing, counselling, and oral PrEP prescription.
Conduct participant assessments, diagnose conditions,
Key Responsibilities:
Interpreting and implementing human resource policies, procedures, rules and regulations.
Providing guidance in matters related to human resource planning, recruitment, s
Key Responsibilities:
Oversee that all study procedures, consent forms, and documentation are completed, verified, and organized per protocol.
Provide daily oversight, guidance, and problem-so
Duties and Responsibilities:
Manage calendars, meetings, and calls
Coordinate with U.S.based collaborators
Anticipate project needs and ensure priorities are well-prepared
Organize local t
Duties and Responsibilities:
Safely transport staff, participants, and study materials while complying with all road safety regulations.
Conduct routine vehicle checks, maintain logbooks, and
Duties and Responsibilities:
Accurately enter participant information and clinical/research data into electronic systems such as ODK, OpenMRS, and REDCap.
Maintain organized participant files,
Duties and Responsibilities:
Identify, mobilize, screen, consent, and enroll eligible participants while providing clear study information and appointment reminders.
Trace and re-engage partic
Duties and Responsibilities:
Screen, consent, enroll, and follow up study participants, ensuring accurate documentation of clinical procedures, adverse events, and visit outcomes.
Provide stud
Duties and Responsibilities:
Develop, implement, and ensure adherence to study protocols, SOPs, and data management plans
Oversee data collection, entry, cleaning, validation, and secure stora
Duties and Responsibilities:
Collect, verify, and accurately document demographic, clinical, and lesion measurement data (including SOC ruler-based ACTG criteria and SS3D imaging).
Implement a
Key Responsibilities:
Make appointments with study participants, administer informed consent and conduct research interviews
Transcribe and translate (if necessary) audio files and submit type
Key Responsibilities:
Dispensing prescribed medications and pharmaceutical preparations
Verifying and maintaining information relating to patients
Ordering and recording of drugs and other s
