{"id":105083,"date":"2026-07-31T07:18:54","date_gmt":"2026-07-31T07:18:54","guid":{"rendered":"https:\/\/jobs.dataaxisnode.com\/kenya\/uncategorized\/study-nurse-kisumu-5-posts\/"},"modified":"2026-07-31T07:18:54","modified_gmt":"2026-07-31T07:18:54","slug":"study-nurse-kisumu-5-posts","status":"publish","type":"post","link":"https:\/\/jobs.dataaxisnode.com\/kenya\/jobs\/kisumu\/study-nurse-kisumu-5-posts\/","title":{"rendered":"Study Nurse &#8211; Kisumu &#8211; 5 Posts"},"content":{"rendered":"<p><script type=\"application\/ld+json\">{\"@context\": \"https:\/\/schema.org\/\", \"@type\": \"JobPosting\", \"title\": \"Study Nurse - Kisumu - 5 Posts\", \"description\": \"Key Responsibilities:\\nRecruit, screen, consent, enroll, and retain study participants in accordance with the study protocol, SOPs, Good Clinical Practice GCP, ethical, and regulatory requirements.\\nConduct study procedures, administer study questionnaires, and collect demographic, behavioral, and clinical data using approved study tools.\\nProvide participant counseling on HIV prevention, STI prevention, contraception, adherence to study products, risk reduction, and other protocol-required health education.\\nCoordinate participant follow-up visits, appointment reminders, tracing, and retention activities to minimize loss to follow-up and ensure protocol compliance.\\nComplete and maintain accurate study documentation, including source documents, case report forms CRFs, participant logs, and timely data entry into REDCap and other approved electronic databases.\\nReview study data and records for completeness, accuracy, and protocol compliance; resolve data queries, and promptly document and report adverse events, protocol deviations, social harms, and other participant safety concerns.\\nCollaborate with laboratory, pharmacy, clinical, qualitative research, and data management teams, and prepare study documentation for monitoring visits, audits, inspections, and quality assurance activities.\\nMaintain participant confidentiality, comply with institutional policies, GCP, Human Subjects Protection, and all applicable regulatory requirements, participate in study trainings and team meetings, and\\nPerform any other study-related duties assigned by the Supervisor.\\nVacancy Requirements:\\nDiploma or Bachelor\u2019s Degree in Nursing from a recognized institution.\u00a0\u00a0 \u00a0Mandatory\\nMinimum of 2\u20133 years' experience in research, clinical trials, or related healthcare settings.\u00a0\u00a0 \u00a0Mandatory\\nValid nursing registration and licensure.\u00a0\u00a0 \u00a0Mandatory\\nCurrent Good Clinical Practice GCP and Human Subjects Protection HSP certification.\u00a0\u00a0 \u00a0Mandatory\\nExcellent verbal and written communication skills.\u00a0\u00a0 \u00a0Skills & Competencies\\nStrong organizational and time-management skills with high attention to detail.\u00a0\u00a0 \u00a0Skills & Competencies\\nAbility to work independently and as part of a multidisciplinary team.\u00a0\u00a0 \u00a0Skills & Competencies\\nGood problem-solving skills, initiative, and resourcefulness.\u00a0\u00a0 \u00a0Skills & Competencies\", \"datePosted\": \"2026-07-31\", \"hiringOrganization\": {\"@type\": \"Organization\", \"name\": \"Kenya Medical Research - KEMRI\"}, \"jobLocation\": {\"@type\": \"Place\", \"address\": {\"@type\": \"PostalAddress\", \"addressLocality\": \"Kisumu\", \"addressCountry\": \"KE\"}}, \"directApply\": true, \"validThrough\": \"2026-08-20T23:59:59\", \"employmentType\": \"CONTRACTOR\"}<\/script><\/p>\n<p><strong>Company:<\/strong> Kenya Medical Research &#8211; KEMRI<\/p>\n<p><strong>Location:<\/strong> Kisumu<\/p>\n<p><strong>Job Type:<\/strong> Contract<\/p>\n<p><strong>Apply Before:<\/strong> 2026-08-20<\/p>\n<h3>Job Description<\/h3>\n<p>Key Responsibilities:<br \/>Recruit, screen, consent, enroll, and retain study participants in accordance with the study protocol, SOPs, Good Clinical Practice GCP, ethical, and regulatory requirements.<br \/>Conduct study procedures, administer study questionnaires, and collect demographic, behavioral, and clinical data using approved study tools.<br \/>Provide participant counseling on HIV prevention, STI prevention, contraception, adherence to study products, risk reduction, and other protocol-required health education.<br \/>Coordinate participant follow-up visits, appointment reminders, tracing, and retention activities to minimize loss to follow-up and ensure protocol compliance.<br \/>Complete and maintain accurate study documentation, including source documents, case report forms CRFs, participant logs, and timely data entry into REDCap and other approved electronic databases.<br \/>Review study data and records for completeness, accuracy, and protocol compliance; resolve data queries, and promptly document and report adverse events, protocol deviations, social harms, and other participant safety concerns.<br \/>Collaborate with laboratory, pharmacy, clinical, qualitative research, and data management teams, and prepare study documentation for monitoring visits, audits, inspections, and quality assurance activities.<br \/>Maintain participant confidentiality, comply with institutional policies, GCP, Human Subjects Protection, and all applicable regulatory requirements, participate in study trainings and team meetings, and<br \/>Perform any other study-related duties assigned by the Supervisor.<br \/>Vacancy Requirements:<br \/>Diploma or Bachelor\u2019s Degree in Nursing from a recognized institution.\u00a0\u00a0 \u00a0Mandatory<br \/>Minimum of 2\u20133 years&#8217; experience in research, clinical trials, or related healthcare settings.\u00a0\u00a0 \u00a0Mandatory<br \/>Valid nursing registration and licensure.\u00a0\u00a0 \u00a0Mandatory<br \/>Current Good Clinical Practice GCP and Human Subjects Protection HSP certification.\u00a0\u00a0 \u00a0Mandatory<br \/>Excellent verbal and written communication skills.\u00a0\u00a0 \u00a0Skills &#038; Competencies<br \/>Strong organizational and time-management skills with high attention to detail.\u00a0\u00a0 \u00a0Skills &#038; Competencies<br \/>Ability to work independently and as part of a multidisciplinary team.\u00a0\u00a0 \u00a0Skills &#038; Competencies<br \/>Good problem-solving skills, initiative, and resourcefulness.\u00a0\u00a0 \u00a0Skills &#038; Competencies<\/p>\n<h3>How to Apply<\/h3>\n<p>Interested and qualified? Go to Kenya Medical Research &#8211; KEMRI on erecruitment.kemri.go.ke to apply<br \/>Build your CV for free. Download in different templates.<\/p>\n<p><a href=\"https:\/\/www.myjobmag.co.ke\/apply-now\/1293659\" 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: MyJobMag<\/small><\/p>\n<p><!-- job-expiry: 2026-08-20 --><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Company: Kenya Medical Research &#8211; KEMRI Location: Kisumu Job Type: Contract Apply Before: 2026-08-20 Job Description Key Responsibilities:Recruit, screen, consent, enroll, and retain study participants in accordance with the study protocol, SOPs, Good Clinical Practice GCP, ethical, and regulatory requirements.Conduct study procedures, administer study questionnaires, and collect demographic, behavioral, and clinical data using approved study [&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":[1443,1413,1637,1412],"class_list":["post-105083","post","type-post","status-publish","format-standard","hentry","category-jobs","category-kisumu","tag-contract","tag-job-listing","tag-kenya-medical-research-kemri","tag-myjobmag"],"_links":{"self":[{"href":"https:\/\/jobs.dataaxisnode.com\/kenya\/wp-json\/wp\/v2\/posts\/105083","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=105083"}],"version-history":[{"count":0,"href":"https:\/\/jobs.dataaxisnode.com\/kenya\/wp-json\/wp\/v2\/posts\/105083\/revisions"}],"wp:attachment":[{"href":"https:\/\/jobs.dataaxisnode.com\/kenya\/wp-json\/wp\/v2\/media?parent=105083"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/jobs.dataaxisnode.com\/kenya\/wp-json\/wp\/v2\/categories?post=105083"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/jobs.dataaxisnode.com\/kenya\/wp-json\/wp\/v2\/tags?post=105083"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}