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:
Assessing study participants and establishing health care needs,
Planning and implementing research related procedures as per specific study protocols,
Providing health
Key Responsibilities:
Maintain studies’ compliance with applicable guidelines and regulations as well as all relevant local laws at all times,
Keep track of all study protocols at the va
Key Responsibilities:
Dispense drugs to study participants.
Counsel clients on drug administration and compliance.
Order corresponding supplies such as drugs, clinical items, and other pharm
Key Responsibilities:
Preparing and dispensing drugs to patients/study participants.
Verify that prescriptions are filled correctly and on time.
Interacting with patients/study participants,
Key Responsibilities:
Implementing clinical research projects and/or supervise designated aspects of the work
Establishing strategic partnerships for research, training, innovations, technolog
Key Responsibilities:
Community engagement and entry
Participant mobilization and recruitment
Informed consent
Cross-sectional surveys
Keeping track of study participants for follow-up a
Key Responsibilities:
Conducting fieldwork for data collection, including surveys and sample collection.
Conducting laboratory experiments to optimize ONT protocols for pathogen de-tection.
Vacancy Requirements:
Bachelor of Science in Biochemistry/Microbiology / Molecular Biology/ Biotechnology/ Genomics or any related biological science course from a recognized institution.
Be F
Key Responsibilities:
Oversee all clinic and other study personnel performing study specific tasks and procedures.
Monitors adverse events and reports them to the safety monitor as required.
Key Responsibilities:
Assist in Research Project: Collaborate with the research team to develop and implement research protocols, including recruiting participants, obtaining informed consent, a
Key Responsibilities:
Participant Recruitment and Screening: Support the recruitment and retention of participants.
Initial Assessment and Evaluation: Conduct initial assessment and evaluation
Key Responsibilities:
Imprest reconciliations and management
Monitor budget through expenditure
Prepare variance reports
Assist in facilitating training & conferences
Monitor & e
Key Responsibilities:
Community sensitization and mobilization for the study.
Work with CORPS to map the study area and recruit potential subjects.
Hold regular meetings and communication wi
Key Responsibilities:
Accurate and timely performance of study-specific assays
Ensuring custody of participant specimens and storage/archival
Appropriate reporting of any abnormal lab result
Key Responsibilities:
Prescreening and screening of participants
Register and consent study participants and assist with eligibility determination, screening, and enrolment of study participan
Key Responsibilities:
Performing Clinical Assessments.
Collecting specimens.
Conducting interviews, administering Case report forms, and form completion
Offer support counseling to study p
Key Responsibilities:
Administer respective Case Report Forms (CRFs
Carrying out QA/QC of study CRFs and source docs and resolve queries that may arise.
Dispensing drugs and Study products t
Key Responsibilities:
Participate in participant review and care, and all study procedures as guided by study protocols.
Perform pelvic exams, cervical cancer screening, contraceptive counsell
