{"id":106706,"date":"2026-08-10T07:21:26","date_gmt":"2026-08-10T07:21:26","guid":{"rendered":"https:\/\/jobs.dataaxisnode.com\/kenya\/uncategorized\/study-nurses-research-care-and-training-program\/"},"modified":"2026-08-10T07:21:26","modified_gmt":"2026-08-10T07:21:26","slug":"study-nurses-research-care-and-training-program","status":"publish","type":"post","link":"https:\/\/jobs.dataaxisnode.com\/kenya\/jobs\/kisumu\/study-nurses-research-care-and-training-program\/","title":{"rendered":"Study Nurses &#8211; Research Care and Training Program"},"content":{"rendered":"<p><script type=\"application\/ld+json\">{\"@context\": \"https:\/\/schema.org\/\", \"@type\": \"JobPosting\", \"title\": \"Study Nurses - Research Care and Training Program\", \"description\": \"University of Washington, Kenya\\nResearch Care and Training Program\\nVacancy Announcement\\nUniversity of Washington, Fred Hutchison Cancer Center and the Ministry of Health funded by NIH is conducting a hybrid effectiveness-implementation cluster-randomized controlled trial to evaluate whether integrating telehealth support into pharmacy-based PrEP and PEP delivery improves clinical and implementation outcomes.\\n\\nThe study will be conducted in 24 private pharmacies across Kisumu, Homa Bay, Migori, Siaya, and Vihiga counties in western Kenya.\\nPosition:\\nStudy Nurse\\n(4 Positions)\\nReports to:\\nStudy Coordinator\\nLocation:\\nKisumu\\nDuration:\\n1 Year Renewable\\nMain Objectives of this position:\\nThis position involves assessment, counseling, informed consent and case management administration and sexual reproductive assessment.\\nKey Responsibilities\\nRecruit, screen, consent, enroll, and retain study participants in accordance with the study protocol, SOPs, and Good Clinical Practice (GCP) guidelines.\\nConduct study activities as outlined in the study protocol and in compliance with applicable SOPs, ethical guidelines, and regulatory requirements.\\nProvide comprehensive counseling on HIV prevention, STI prevention, contraception, adherence to study products, and risk-reduction strategies.\\nAdminister study questionnaires and collect demographic, behavioral, and clinical information using approved study tools.\\nCoordinate participant follow-up visits, appointment reminders, participant tracing, and retention activities to minimize loss to follow-up.\\nAccurately complete study source documents, case report forms (CRFs), screening logs, enrollment logs, participant tracking logs, and visit documentation.\\nAccurately enter participant information and study data into electronic data capture systems including REDCap and other study databases as required.\\nReview study records for completeness, accuracy, and protocol compliance and resolve data queries in collaboration with the data management team.\\nEnsure timely reporting and documentation of adverse events, protocol deviations, social harms, and participant safety concerns.\\nCollaborate closely with laboratory, pharmacy, qualitative research, data management, and clinical teams to ensure smooth implementation of study activities.\\nPrepare study documentation for monitoring visits, audits, inspections, and quality assurance reviews.\\nMaintain participant confidentiality and uphold ethical standards throughout all study activities.\\nParticipate in study trainings, team meetings, refresher trainings, and protocol update sessions.\\nEnsure compliance with study protocols, institutional policies, GCP, Human Subjects Protection requirements, and applicable regulatory guidelines.\\nPerform any other study-related duties assigned by the Study Coordinator.\\nQualifications and Experience\\nDiploma or Bachelor\u2019s Degree in Nursing from a recognized institution.\\nMinimum of 2\u20133 years' experience in research, clinical trials, or related healthcare settings.\\nValid nursing registration and licensure.\\nCurrent Good Clinical Practice (GCP) and Human Subjects Protection (HSP) certification.\\nRequired Competencies\\nExcellent verbal and written communication skills.\\nStrong organizational and time-management skills with high attention to detail.\\nAbility to work independently and as part of a multidisciplinary team.\\nGood problem-solving skills, initiative, and resourcefulness.\\nSuccessful candidates will be required to provide the following:\\nCertificate of good conduct, Higher Education Loans Board compliance certificate, KRA Tax compliance certificate, Credit Reference Bureau clearance certificate, and Ethics and Anti-Corruption Commission clearance, testimonials and other\\nrelevant documents.\\n\\nAll the applications to be done through\\nTHIS LINK\\non or before 14th August 2026 latest 5.00 p.m.\\n\\nWE ARE EQUAL OPPORTUNITY EMPLOYER COMMITTED TO DIVERSITY; PERSONS WHO ARE ABLED DIFFERENTLY, WOMEN, YOUTH AND THOSE FROM MARGINALIZED AREAS ARE ENCOURAGED TO APPLY. DIRECT OR INDIRECT CANVASSING WILL LEAD TO AUTOMATIC DISQUALIFICATION. WE DOES NOT CHARGE A FEE AT ANY STAGE OF ITS RECRUITMENT PROCESS INCLUDING APPLICATION, INTERVIEW AND PROCESSING OF OFFER LETTER. IF ASKED FOR A FEE, REPORT SUCH REQUEST IMMEDIATELY.\\n\\nOnly shortlisted candidates will be contacted\", \"datePosted\": \"2026-08-06\", \"hiringOrganization\": {\"@type\": \"Organization\", \"name\": \"University of Washington, Kenya\"}, \"jobLocation\": {\"@type\": \"Place\", \"address\": {\"@type\": \"PostalAddress\", \"addressLocality\": \"Kisumu\", \"addressCountry\": \"KE\"}}, \"directApply\": true, \"validThrough\": \"2026-08-27T23:59:59\", \"employmentType\": \"FULL_TIME\"}<\/script><\/p>\n<p><strong>Company:<\/strong> University of Washington, Kenya<\/p>\n<p><strong>Location:<\/strong> Kisumu<\/p>\n<p><strong>Job Type:<\/strong> Full-time<\/p>\n<p><strong>Apply Before:<\/strong> 2026-08-27<\/p>\n<h3>Job Description<\/h3>\n<p>University of Washington, Kenya<br \/>Research Care and Training Program<br \/>Vacancy Announcement<br \/>University of Washington, Fred Hutchison Cancer Center and the Ministry of Health funded by NIH is conducting a hybrid effectiveness-implementation cluster-randomized controlled trial to evaluate whether integrating telehealth support into pharmacy-based PrEP and PEP delivery improves clinical and implementation outcomes.<\/p>\n<p>The study will be conducted in 24 private pharmacies across Kisumu, Homa Bay, Migori, Siaya, and Vihiga counties in western Kenya.<br \/>Position:<br \/>Study Nurse<br \/>(4 Positions)<br \/>Reports to:<br \/>Study Coordinator<br \/>Location:<br \/>Kisumu<br \/>Duration:<br \/>1 Year Renewable<br \/>Main Objectives of this position:<br \/>This position involves assessment, counseling, informed consent and case management administration and sexual reproductive assessment.<br \/>Key Responsibilities<br \/>Recruit, screen, consent, enroll, and retain study participants in accordance with the study protocol, SOPs, and Good Clinical Practice (GCP) guidelines.<br \/>Conduct study activities as outlined in the study protocol and in compliance with applicable SOPs, ethical guidelines, and regulatory requirements.<br \/>Provide comprehensive counseling on HIV prevention, STI prevention, contraception, adherence to study products, and risk-reduction strategies.<br \/>Administer study questionnaires and collect demographic, behavioral, and clinical information using approved study tools.<br \/>Coordinate participant follow-up visits, appointment reminders, participant tracing, and retention activities to minimize loss to follow-up.<br \/>Accurately complete study source documents, case report forms (CRFs), screening logs, enrollment logs, participant tracking logs, and visit documentation.<br \/>Accurately enter participant information and study data into electronic data capture systems including REDCap and other study databases as required.<br \/>Review study records for completeness, accuracy, and protocol compliance and resolve data queries in collaboration with the data management team.<br \/>Ensure timely reporting and documentation of adverse events, protocol deviations, social harms, and participant safety concerns.<br \/>Collaborate closely with laboratory, pharmacy, qualitative research, data management, and clinical teams to ensure smooth implementation of study activities.<br \/>Prepare study documentation for monitoring visits, audits, inspections, and quality assurance reviews.<br \/>Maintain participant confidentiality and uphold ethical standards throughout all study activities.<br \/>Participate in study trainings, team meetings, refresher trainings, and protocol update sessions.<br \/>Ensure compliance with study protocols, institutional policies, GCP, Human Subjects Protection requirements, and applicable regulatory guidelines.<br \/>Perform any other study-related duties assigned by the Study Coordinator.<br \/>Qualifications and Experience<br \/>Diploma or Bachelor\u2019s Degree in Nursing from a recognized institution.<br \/>Minimum of 2\u20133 years&#8217; experience in research, clinical trials, or related healthcare settings.<br \/>Valid nursing registration and licensure.<br \/>Current Good Clinical Practice (GCP) and Human Subjects Protection (HSP) certification.<br \/>Required Competencies<br \/>Excellent verbal and written communication skills.<br \/>Strong organizational and time-management skills with high attention to detail.<br \/>Ability to work independently and as part of a multidisciplinary team.<br \/>Good problem-solving skills, initiative, and resourcefulness.<br \/>Successful candidates will be required to provide the following:<br \/>Certificate of good conduct, Higher Education Loans Board compliance certificate, KRA Tax compliance certificate, Credit Reference Bureau clearance certificate, and Ethics and Anti-Corruption Commission clearance, testimonials and other<br \/>relevant documents.<\/p>\n<p>All the applications to be done through<br \/>THIS LINK<br \/>on or before 14th August 2026 latest 5.00 p.m.<\/p>\n<p>WE ARE EQUAL OPPORTUNITY EMPLOYER COMMITTED TO DIVERSITY; PERSONS WHO ARE ABLED DIFFERENTLY, WOMEN, YOUTH AND THOSE FROM MARGINALIZED AREAS ARE ENCOURAGED TO APPLY. DIRECT OR INDIRECT CANVASSING WILL LEAD TO AUTOMATIC DISQUALIFICATION. WE DOES NOT CHARGE A FEE AT ANY STAGE OF ITS RECRUITMENT PROCESS INCLUDING APPLICATION, INTERVIEW AND PROCESSING OF OFFER LETTER. IF ASKED FOR A FEE, REPORT SUCH REQUEST IMMEDIATELY.<\/p>\n<p>Only shortlisted candidates will be contacted<\/p>\n<h3>How to Apply<\/h3>\n<p>THIS LINK<\/p>\n<p><a href=\"https:\/\/docs.google.com\/forms\/d\/e\/1FAIpQLSdK2-vXKqU-kb-IHh4PJcowz4W0ozV5vlWbcX9E2LybKJNqUw\/viewform\" target=\"_blank\" rel=\"noopener\" style=\"display:inline-block;padding:10px 20px;background:#2271b1;color:#fff;text-decoration:none;border-radius:4px;\">Apply Now<\/a><\/p>\n<p><small>Source: JobsInKenya<\/small><\/p>\n<p><!-- job-expiry: 2026-08-27 --><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Company: University of Washington, Kenya Location: Kisumu Job Type: Full-time Apply Before: 2026-08-27 Job Description University of Washington, KenyaResearch Care and Training ProgramVacancy AnnouncementUniversity of Washington, Fred Hutchison Cancer Center and the Ministry of Health funded by NIH is conducting a hybrid effectiveness-implementation cluster-randomized controlled trial to evaluate whether integrating telehealth support into pharmacy-based PrEP [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[1408,1571],"tags":[1654,1413,1656,2775],"class_list":["post-106706","post","type-post","status-publish","format-standard","hentry","category-jobs","category-kisumu","tag-full-time-2","tag-job-listing","tag-jobsinkenya","tag-university-of-washington-kenya"],"_links":{"self":[{"href":"https:\/\/jobs.dataaxisnode.com\/kenya\/wp-json\/wp\/v2\/posts\/106706","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/jobs.dataaxisnode.com\/kenya\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/jobs.dataaxisnode.com\/kenya\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/jobs.dataaxisnode.com\/kenya\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/jobs.dataaxisnode.com\/kenya\/wp-json\/wp\/v2\/comments?post=106706"}],"version-history":[{"count":0,"href":"https:\/\/jobs.dataaxisnode.com\/kenya\/wp-json\/wp\/v2\/posts\/106706\/revisions"}],"wp:attachment":[{"href":"https:\/\/jobs.dataaxisnode.com\/kenya\/wp-json\/wp\/v2\/media?parent=106706"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/jobs.dataaxisnode.com\/kenya\/wp-json\/wp\/v2\/categories?post=106706"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/jobs.dataaxisnode.com\/kenya\/wp-json\/wp\/v2\/tags?post=106706"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}