Latest Recruitment at Kenya Medical Research - KEMRI

Key Responsibilities:

• The interns will be trained on logistics for project activities, including transportation, procurement, inventory and office organization among other duties.
• The interns will be trained on administrative tasks such as data entry, documentation, and record-keeping.
• The interns will be trained on communication between project teams, suppliers, and other stakeholders.
• The interns will be trained on packaging and distribution of study materials and equipment as required.
• The interns will be trained on organizing meetings, workshops, and field activities.
• The interns will be trained on any other duties as assigned to support project operations.

Vacancy Requirements:

• Certificate in Business Administration, Logistics, Procurement, or a related field    Mandatory
• Basic computer proficiency (Microsoft Office applications).    Mandatory
• Willing to live and work in Kisumu    Mandatory
• Willingness to learn and develop personal quarterly reports of knowledge and skills gained    Mandatory
• Strong organizational and time management skills.    Mandatory
• Excellent communication and interpersonal skills.    Mandatory
• Ability to work as part of a team    Mandatory
• Excellent communication skills – interpersonal, written, and verbal    Mandatory
• Ability to multitask and flexibility are desirable attributes    Mandatory
• Strong communication and organizational skills and detail-oriented    Mandatory

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Key Responsibilities:

• The interns will be trained on logistics for project activities, including transportation, procurement, inventory and office organization among other duties.
• The interns will be trained on administrative tasks such as data entry, documentation, and record-keeping.
• The interns will be trained on communication between project teams, suppliers, and other stakeholders.
• The interns will be trained on packaging and distribution of study materials and equipment as required.
• The interns will be trained on organizing meetings, workshops, and field activities.
• The interns will be trained on any other duties as assigned to support project operations.

Vacancy Requirements:

• Certificate in Business Administration, Logistics, Procurement, or a related field    Mandatory
• Basic computer proficiency (Microsoft Office applications).    Mandatory
• Willing to live and work in Kisumu    Mandatory
• Willingness to learn and develop personal quarterly reports of knowledge and skills gained    Mandatory
• Strong organizational and time management skills.    Mandatory
• Excellent communication and interpersonal skills.    Mandatory
• Ability to work as part of a team    Mandatory
• Excellent communication skills – interpersonal, written, and verbal    Mandatory
• Ability to multitask and flexibility are desirable attributes    Mandatory
• Strong communication and organizational skills and detail-oriented    Mandatory

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Key Responsibilities:

• Greet and assist participants, visitors, and staff in a friendly and professional manner.
• Manage front desk operations, including answering phones, scheduling participant appointments, attending to visitors, and handling inquiries.
• Register study participants and update existing participants records accurately.
• Coordinate with clinical and research teams to ensure smooth clinic operations.
• Provide information about clinic services, including FP/PrEP services, and direct participants to appropriate resources.
• Maintain confidentiality of participant information in compliance with Research Ethics and Site’s policies.

Vacancy Requirements:

• Diploma in Front Office or equivalent    Mandatory
• Additional certification in office administration or related field    Added Advantage
• Excellent communication and interpersonal skills.    Mandatory
• Strong organizational and multitasking abilities.    Mandatory
• Computer literate    Mandatory
• Ability to maintain confidentiality and handle sensitive information.    Mandatory
• Basic knowledge of HIV prevention, including oral PrEP, is an advantage    Added Advantage
• Friendly, empathetic, and patient-centered approach.    Mandatory
• Ability to work in a fast-paced, research-focused environment    Mandatory

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Key Responsibilities:

• Provide high-quality clinical care to participants, including HIV testing, counselling, and prescription of oral PrEP.
• Conduct participants assessments, diagnose medical conditions, and develop treatment plans in line with the study protocol protocols.
• Support the implementation and monitoring of clinical procedures related to the study protocol.
• Educate participants on HIV prevention, PrEP adherence, and sexual health.
• Collaborate with the research team to collect, document, and report clinical data accurately.
• Ensure compliance with ethical, regulatory, and clinical guidelines in all activities.
• Safety assessment and reporting
• Perform Phlebotomy, and contraceptive method administration and Sexual Reproductive Health Assessments
• Administer respective Case Report Forms (CRFs)
• Carrying out QA/QC of study CRFs, source docs, and resolve queries that may arise.
• Develop and review of study related related SOPs
• Participate in training and capacity-building activities for clinic staff and community partners.
• Maintain accurate and confidential participants records in compliance with Site’s policies and regulations.

Vacancy Requirements:

• Bachelor of Medicine and Bachelor of Surgery (MBChB) or equivalent medical degree    Mandatory
• Valid practicing license    Mandatory
• Minimum of 2–3 years of clinical experience, preferably in HIV care, sexual health, or infectious diseases.    Mandatory
• Experience in research settings or clinical trials is highly desirable.    Mandatory
•  Familiarity with Contraceptive method administration, PrEP ,PrEP guidelines and HIV prevention strategies/interventions is a plus.    Mandatory
• Strong clinical and diagnostic skills.    Mandatory
• Excellent communication and patient counselling skills.    Mandatory
• Ability to work effectively in a multidisciplinary team    Mandatory
• Proficiency in electronic medical records (EMR) and data management systems.    Mandatory
• Knowledge of ethical and regulatory requirements for clinical research.    Mandatory
• Compassionate, patient-cantered approach to care.    Mandatory
• Strong organizational and time-management skills.    Mandatory
• Commitment to advancing public health and HIV prevention    Mandatory
• Ability to oversee/supervise a team    Mandatory
• Good Clinical Practice (GCP) and Human Subject Protection (HSP) certification with Strong knowledge of ICH guidelines, FDA, PPB, and other global regulatory frameworks    Mandatory

go to method of application »

Key Responsibilities:

• Provide high-quality clinical care to participants, including HIV testing, counselling, and prescription of oral PrEP.
• Perform Phlebotomy, and contraceptive method administration and Sexual Reproductive Health Assessments
• Conduct participant assessments, eligibility, diagnose medical conditions, and develop treatment plans in line with the study protocol.
• Support the implementation and monitoring clinic activities related to HIV prevention and oral PrEP.
• Educate participants on HIV prevention, PrEP adherence, and sexual health.
• Collaborate with the research team to collect, document, and report clinical data accurately.
• Ensure compliance with ethical, regulatory, and clinical guidelines in all activities.
• Participate in training and capacity-building activities for clinic staff and community partners.
• Informed Consent form administration
• Administer respective Case Report Forms (CRFs)
• Carrying out QA/QC of study CRFs, source docs, and resolve queries that may arise.
• Develop and review of clinic related related SOPs

Vacancy Requirements:

• Diploma in Clinical Medicine and Surgery or equivalent.    Mandatory
• Valid clinical officer license to practice in Kenya.    Mandatory
• Additional training in HIV care, Sexual Reproductive Health, or public health is an advantage    Added Advantage
• Minimum of 2–3 years of clinical experience, preferably in HIV care, sexual health, or infectious diseases.    Mandatory
• Experience in research settings or clinical trials is highly desirable.    Mandatory
• Familiarity with FP/PrEP and HIV prevention strategies is a plus.    Mandatory
• Strong clinical and diagnostic skills.    Mandatory
• Excellent communication and patient counselling skills.    Mandatory
• Ability to work effectively in a multidisciplinary team.    Mandatory
• Proficiency in electronic medical records (EMR) and data management systems.    Mandatory
• Knowledge of ethical and regulatory requirements for clinical research.    Mandatory
• Compassionate, patient-centred approach to care.    Mandatory
• Strong organizational and time-management skills.    Mandatory
• Commitment to advancing public health and HIV prevention.    Mandatory
• Good Clinical Practice (GCP) and Human Subject Protection (HSP) certification with Strong knowledge of ICH guidelines    Mandatory
• Maintain accurate and confidential participants records in compliance with site policies and regulations.    Mandatory

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Key Responsibilities:

• Assist in the dispensing of medications, including oral PrEP, under the supervision of a licensed pharmacist.
• Manage pharmacy inventory, including ordering, receiving, and storing medications and supplies to prevent shortages and overstocking.
• Maintain accurate records of medication dispensing and inventory levels.
• Provide education to participants on medication use, including oral PrEP adherence and potential side effects.
• Ensure proper storage conditions for Study Investigational product and other medications, adhering to safety and quality assurance standards.
• Support the research team by preparing and dispensing study medications as per protocol requirements.
• Ensure compliance with pharmacy regulations, clinic policies, and research protocols.
• Collaborate with the clinical and research teams to ensure smooth clinic operations.
• Maintain a clean, organized, and safe pharmacy environment.
• Administer respective Case Report Forms (CRFs)
• Carrying out QA/QC of study CRFs, source docs, and resolve queries that may arise.
• Maintaining pharmacy temperature and humidity logs
• Participants Randomization process in liaison with the data and clinic teams.
• Generation and review of pharmacy SOP’s and ensuring adherence to the same
• Processing shipment documentation of study products and track study product shipment from source to site.
• Processing study products destruction documents and taking part in actual destruction process.
• Enhancing communication between pharmacy and local PPB and coordinating center.
• Management of regulatory affairs regarding pharmacy

Vacancy Requirements:

• Diploma or certificate in Pharmacy Technology or related field.    Mandatory
• Valid pharmacy technologist license to practice in Kenya    Mandatory
• Additional training in HIV care or public health is an advantage.    Added Advantage
• Minimum of 1–2 years of experience as a pharmacy technologist, preferably in a clinical or research setting.    Mandatory
• Experience with HIV medications, including oral PrEP, is highly desirable.    Mandatory
• Familiarity with inventory management systems and electronic medical records (EMR) is a plus.    Mandatory
• Strong knowledge of pharmacy operations and medication dispensing    Mandatory
• Excellent attention to detail and organizational skills.    Mandatory
• Ability to work effectively in a multidisciplinary team.    Mandatory
• Good communication and patient counselling skills.    Mandatory
• Knowledge of ethical and regulatory requirements for clinical research.    Mandatory
• Compassionate and patient-centred approach to care.    Mandatory
• Strong problem-solving and time-management skills    Mandatory
• Commitment to advancing public health and HIV prevention.    Mandatory
• Good Clinical Practice (GCP) and Human Subject Protection (HSP) certification with Strong knowledge of ICH guidelines, FDA, PPB, and other global regulatory frameworks    Mandatory

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Key Responsibilities:

• Provide high-quality nursing care to participants, including HIV counseling, adherence counseling and tracking of PrEP and contraceptives.
• Conduct participants assessments, monitor vital signs, and assist in the diagnosis and treatment of medical conditions.
• Educate participants on HIV prevention, PrEP adherence, and sexual health.
• Support the implementation and monitoring of research studies related to HIV prevention and oral PrEP.
• Informed Consent administration
• Collaborate with the research team to collect, document, and report clinical data accurately.
• Administer Case Report Forms and perform quality checks
• Ensure compliance with ethical, regulatory, and clinical guidelines in all activities.
• Participate in training and capacity-building activities for clinic staff and community partners.
• Maintain accurate and confidential participants records in compliance with site policies and regulations.
• Perform participant off site visits
• Perform Phlebotomy and Sexual Reproductive assessments
• Develop and review of clinic related related SOPs

Vacancy Requirements:

• Diploma or degree in Nursing from an accredited institution.    Mandatory
• Valid nursing license to practice in Kenya.    Mandatory
• Additional training in HIV care, sexual health, or public health is an advantage    Added Advantage
• Minimum of 2–3 years of nursing experience, preferably in HIV care, sexual health, or infectious diseases.    Mandatory
• Experience in research settings or clinical trials is highly desirable.    Mandatory
• Familiarity with FP/PrEP and HIV prevention strategies is a plus.    Mandatory
• Strong clinical and diagnostic skills.    Mandatory
• Excellent communication and patient counseling skills.    Mandatory
• Ability to work effectively in a multidisciplinary team.    Mandatory
• Proficiency in electronic medical records (EMR) and data management systems.    Mandatory
• Knowledge of ethical and regulatory requirements for clinical research.    Mandatory
• Compassionate, patient-centered approach to care.    Mandatory
• Strong organizational and time-management skills.    Mandatory
• Commitment to advancing participant care and HIV prevention.    Mandatory
• Good Clinical Practice (GCP) and Human Subject Protection (HSP) certification with Strong knowledge of ICH guidelines    Mandatory

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Key Responsibilities:

• Develop and implement data management plans for the study.
• Design and maintain electronic data capture (EDC) systems and databases.
• Ensure accurate and timely data entry, cleaning, and validation.
• Monitor data quality and resolve discrepancies in collaboration with the research team.
• Generate reports and data summaries for study monitoring and regulatory submissions.
• Ensure compliance with data protection regulations, ethical guidelines, and study protocols.
• Train and support clinic staff on data collection and management procedures.
• Collaborate with researchers, statisticians, and other stakeholders to support data analysis and interpretation.
• Maintain confidentiality and security of all research data.
• Develop and review of data related SOPs

Vacancy Requirements:

• Bachelor’s Degree in Data Management, Biostatistics, Computer Science, or a related field.    Mandatory
• Strong knowledge of data management principles and practices.    Mandatory
• Proficiency in statistical software (e.g., SPSS, Stata, R) and Microsoft Excel.    Mandatory
• Excellent attention to detail and problem-solving skills.    Mandatory
• Ability to work effectively in a multidisciplinary team.    Mandatory

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Key Responsibilities:

• Perform routine data quality checks to ensure accuracy and completeness of Case Report Forms (CRFs).
• Assist in maintaining and organizing paper and eCRFs and source documents.
• Support the data management team in cleaning, validating, and resolving data discrepancies.
• Generate basic reports and summaries as required by the research team.
• Ensure compliance with data protection policies and confidentiality requirements.
• Assist in the preparation of data for analysis and reporting.
• Collaborate with clinic staff to ensure timely and accurate data collection.
• Data entry
• Ensure data entry computers and all equipment in data room are secure and used appropriately.
• Develop and review of data related SOPs
• Perform other administrative tasks as assigned to support clinic operations.

Vacancy Requirements:

• Diploma or certificate in Data Management, Information Technology or a related field.    Mandatory
• Additional training in data entry or database management is an advantage.    Added Advantage
• Minimum of 1–2 years of experience in data entry or clerical work, preferably in a clinical or research setting.    Mandatory
• Familiarity with electronic data capture (EDC) systems or database software (e.g., REDCap, Excel) is a plus.    Mandatory
• Experience in HIV prevention services, including oral PrEP, is desirable but not required.    Added Advantage
• Strong data entry skills with high accuracy and attention to detail.    Mandatory
• Proficiency in Microsoft Office (Excel, Word) and basic database software.    Mandatory
• Good organizational and time-management skills.    Mandatory
• Ability to work effectively in a team and follow instructions.    Mandatory
• Basic understanding of data confidentiality and ethical guidelines.    Mandatory
• Reliable, diligent, and detail-oriented.    Mandatory

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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.
• Maintain cleaning equipment and supplies, and report any shortages or malfunctions.
• Ensure compliance with infection control and hygiene standards.
• Deliver documents, packages, and supplies to designated locations within and outside the clinic.
• Run errands as assigned by management to support daily operations.
• Assist with setting up rooms for meetings, training sessions, or events.
• Perform minor maintenance tasks, such as replacing light bulbs or reporting repair needs.
• Support clinic staff with other tasks as needed.

Vacancy Requirements:

• Minimum of secondary education.    Mandatory
• Previous experience in cleaning, administrative assistants’ roles, or messenger roles is preferred.    Added Advantage
• Experience working in a healthcare or research setting is a plus.    Mandatory
• Strong attention to detail and cleanliness.    Mandatory
• Ability to follow instructions and work independently.    Mandatory
• Good time-management and organizational skills.    Mandatory
• Basic communication skills in English is required.    Mandatory
• Reliable, punctual, and hardworking.    Mandatory
• Willingness to learn and adapt to clinic protocols.    Mandatory
• Physical ability to perform cleaning tasks and lift/move light to moderate loads.    Mandatory
• Willingness to undergo training on clinic hygiene and safety protocols.    Mandatory
• Flexibility to work occasional evenings or weekends, if required.    Mandatory
• Good Clinical Practice (GCP) and Human Subject Protection (HSP) certification    Mandatory

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Key Responsibilities:

• Perform laboratory tests, including HIV testing and other diagnostic assays per study protocol.
• Prepare and process samples for analysis, ensuring accuracy and adherence to protocols.
• Operate, calibrate, and maintain laboratory equipment and instruments.
• Ensure compliance with laboratory safety protocols and infection control measures.
• Maintain accurate records of laboratory tests, results, and inventory.
• Support the research team by conducting laboratory tests for study participants and ensuring data integrity.
• Assist in the development and implementation of laboratory protocols and procedures.
• Participate in quality control and quality assurance activities to maintain laboratory standards.

Vacancy Requirements:

• Diploma in Medical Laboratory Science, Biomedical Science, or a related field.    Mandatory
• Registered with the regulatory Board-KMLLTB.    Mandatory
• Additional training in HIV testing or molecular diagnostics is an advantage.    Added Advantage
• Minimum of 2–3 years of experience as a laboratory technologist, preferably in a clinical or research setting.    Mandatory
•  Familiarity with Good Clinical Laboratory Practice (GCLP) and research protocols is a plus.    Mandatory
• Strong technical skills in laboratory testing and equipment operation.    Mandatory
• Excellent attention to detail and accuracy in sample processing and data recording.    Mandatory
• Ability to work effectively in a multidisciplinary team.    Mandatory
• Proficiency in laboratory information management systems (LIMS) and data management software.    Mandatory
• Knowledge of laboratory safety protocols and infection control measures.    Mandatory
• Detail-oriented, organized, and proactive.    Mandatory
• Strong problem-solving and time-management skills.    Mandatory

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Key Responsibilities:

• Develop and implement community engagement strategies to raise awareness about Research, SRH, Contraceptives, PrEP and the research study.
• Build and maintain strong relationships with community leaders, organizations, and stakeholders.
• Organize and facilitate community outreach events, workshops, and informational sessions.
• Serve as the primary point of contact for community members, addressing questions, concerns, and feedback about the research study.
• Collaborate with the research team to ensure community perspectives are integrated into study design and implementation.
• Monitor and evaluate community engagement activities to ensure effectiveness and inclusivity.
• Advocate for the needs and interests of the community within the research clinic.
• Maintain accurate records of community interactions and outreach activities.
• Ensure participant recruitment and retention activities are in line with the site
• Oversee, mentor and support the outreach team in their community engagement and participant recruitment/retention efforts.
• Represent the study management in community meetings
• Establish and coordinate the site's CAB and related activities as per the CAB Standard Operating Procedure (SOP).
• Formulate the study recruitment and retention plans, monitor & evaluate and provide technical support to achieve study targets.

Vacancy Requirements:

• Bachelor’s degree in Public Health, Social Work, Communications, or a related field (or equivalent experience).    Mandatory
• Minimum of 2 years of experience in community engagement, public health, or a related role.    Mandatory
• Strong understanding of HIV prevention, FP/PrEP, and related public health issues.    Mandatory
• Excellent communication, interpersonal, and public speaking skills.    Mandatory
• Ability to work effectively with diverse populations, including vulnerable groups.    Mandatory
• Strong organizational skills and the ability to manage multiple tasks simultaneously.    Mandatory
• Proficiency in local language is an asset.    Mandatory
• Knowledge of research ethics and Good Participatory Practice is a plus.    Mandatory
• Good Clinical Practice (GCP) and Human Subject Protection (HSP) certification    Mandatory
• Excellent verbal and written communication skills.    Mandatory
• Ability to convey complex medical and scientific information in an accessible and culturally appropriate manner.    Mandatory
• Strong public speaking and presentation skills.    Mandatory
• Ability to build trust and rapport with diverse populations, including marginalized and at-risk communities.    Mandatory
• Empathy, active listening, and conflict resolution skills.    Mandatory
• Demonstrated understanding of cultural, social, and economic factors affecting health behaviors.    Mandatory
• Experience working with diverse communities and vulnerable groups.    Mandatory
• Strong planning, time management, and multitasking abilities.    Mandatory
• Ability to manage multiple projects and meet deadlines.    Mandatory
• Experience working collaboratively with multidisciplinary teams.    Mandatory
• Strong advocacy skills to represent community needs within the research team.    Mandatory
•  Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).    Mandatory
• Familiarity with data collection and reporting tools is a plus.    Mandatory
• Master’s Degree is an added advantage.    Added Advantage

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Key Responsibilities:

• Track and locate study participants who may have missed follow-up visits or lost contact with the clinic.
• Community entry and engagement
• Participant mobilization and recruitment
• Conduct home visits, phone calls, and community outreach to re-engage participants.
• Maintain accurate and up-to-date records of participant contact information and tracking efforts.
• Perform reminder calls and other participant retention strategies
• Collaborate with the research team to identify and address barriers to participant retention.
• Provide participants with information about the study, appointment reminders, and support as needed.
• Build and maintain positive relationships with participants and the community to foster trust and engagement.
• Ensure all tracking activities are conducted in a culturally sensitive and ethical manner.
• Assist with data entry and reporting related to participant tracking efforts.

Vacancy Requirements:

• Diploma in Public Health, Social Sciences, or a related field is a plus.    Mandatory
• Minimum of 1-2 years of experience in community outreach, participant tracking, or a related role.    Mandatory
• Strong understanding of HIV prevention, PrEP, and related public health issues is preferred.    Mandatory
• Proficiency in local languages is an asset.    Mandatory
• Knowledge of research ethics and confidentiality protocols is a plus.    Mandatory
• Excellent verbal and written communication skills.    Mandatory
• Ability to communicate effectively with diverse populations, including marginalized and at-risk communities.    Mandatory
• Strong interpersonal skills to build trust and rapport with participants.    Mandatory
• Strong attention to detail and ability to maintain accurate records.    Mandatory
• Ability to manage multiple tasks and prioritize effectively.    Mandatory
• Ability to identify and address barriers to participant retention.    Mandatory
• Creative and resourceful in locating hard-to-reach participants.    Mandatory
• Demonstrated understanding of cultural, social, and economic factors affecting health behaviors.    Mandatory
• Experience working with diverse communities and vulnerable groups.    Mandatory
• Familiarity with data collection tools and databases is a plus.    Mandatory
• Ability to work effectively as part of a multidisciplinary team.    Mandatory
• Strong sense of accountability and commitment to study goals.    Mandatory

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Key Responsibilities:

• Develop and manage the study budget in collaboration with the research team.
• Monitor and track study expenses, ensuring alignment with the approved budget.
• Prepare and submit accurate financial reports to management.
• Process invoices, reimbursements, and payments related to study activities.
• Ensure compliance with grant requirements, institutional policies, and regulatory guidelines.
• Collaborate with the research team to forecast financial needs and identify potential risks.
• Maintain accurate and organized financial records for auditing purposes.
• Reports to the Project Finance Manager

Vacancy Requirements:

• Bachelor’s Degree in commerce, Finance, Accounting, Business Administration, or equivalent.    Mandatory
• CPA II certification or equivalent.    Mandatory
• Experience with funds management and compliance is highly desirable.    Mandatory
• Proficiency in financial software (e.g., QuickBooks) and advanced Excel skills.    Mandatory
• Strong organizational and time management skills.    Mandatory
• Ability to analyze data and prepare detailed reports.    Mandatory
• High integrity and ethical governance.    Mandatory
• Excellent communication and administrative skills.    Mandatory
• Good Clinical Practice (GCP) and Human Subject Protection (HSP) certification    Mandatory

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Key Responsibilities:

• Work closely with colleagues and study coordinator to deliver research activities.
• Collect quantitative and qualitative data from a variety of sources.
• Assist with data quality checks and data management.
• Prepare individual work progress reports.
• Comply with policies on ethical conduct of research and human subjects’ protection.
• Carry out any other duties commensurate with experience, which may be assigned from time to time.

Vacancy Requirements:

• Bachelor’s Degree in any of the following disciplines: - Applied Sciences, Public Health, Social Science, or equivalent qualifications from a recognized institution.    Mandatory
• At least two (2) years post-graduate work experience in a relevant research-related position.    Mandatory
• Competency in using Microsoft Excel, Word, and PowerPoint.     Mandatory
• Fluency in English, Kiswahili, required. Maasai Language is an added advantage.    Added Advantage
• Experience in qualitative research methods is an added advantage.    Added Advantage
• Experience with management and processing of qualitative data is an added advantage    Added Advantage
• Familiarity with electronic data collection tools is an added advantage.    Added Advantage
• Ability and willingness to work anywhere in Kajiado County.    Mandatory
• Excellent communication and interpersonal skills.    Mandatory
• Ability to work independently and effectively.    Mandatory
• Ability to interact with study participants in a culturally sensitive manner.    Mandatory
• Well-developed troubleshooting capacity and clarity of thought.    Mandatory
• Strong organization skills to meet tight deadlines.    Mandatory
• Team player    Mandatory

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Key Responsibilities:

• Work closely with study investigators to plan and deliver the research work.
• Prepare study materials including training materials and standard operating procedures.
• Prepare work plans aligned to project deliverables.
• Co-ordinate and oversee data collection and management including data quality checks, storage and archiving.
• Supervise research assistants attached to the Project.
• Co-ordinate adherence to funder’s technical and financial requirements.
• Ensure compliance with policies on ethical conduct of research and human subjects protections.
• Carry out any other duties which may be assigned from time to time.

Vacancy Requirements:

• Bachelor’s Degree in any of the following disciplines: - Biomedical Sciences, Applied Sciences, Public Health, any relevant Social Science, or equivalent qualifications from a recognized institution.    Mandatory
• Master’s Degree in any of the following disciplines: - Biomedical Sciences, Applied Sciences, Public Health, any relevant Social Science, or equivalent qualifications from a recognized institution.    Mandatory
• At least four (4) years of relevant hands-on experience working in field-based studies.    Mandatory
• Competent use of MS Office applications. Experience in electronic data collection and management is an added advantage.    Added Advantage
• Fluency in English, Kiswahili, required. Maasai Language is an added advantage.    Added Advantage
• Experience in participatory research methods is an added advantage.    Added Advantage
• Prior experience in a similar post is an added advantage.    Added Advantage
• Ability and willingness to work anywhere in Kajiado County.    Mandatory
• Excellent verbal and written communication skills.    Mandatory
• Strong organization skills, ability to effectively troubleshoot and respond to a dynamic work environment.    Mandatory
• Independent judgment and resourcefulness, understanding of the local social and geographical landscape as well as the community.    Mandatory
• Detail-oriented with good reporting skills.    Mandatory
• Strong communication skills.    Mandatory