{"version":"0.1","company":{"name":"YubHub","url":"https://yubhub.co","jobsUrl":"https://yubhub.co/jobs/city/kor-client/"},"x-facet":{"type":"city","slug":"kor-client","display":"Kor-client","count":2},"x-feed-size-limit":100,"x-feed-sort":"enriched_at desc","x-feed-notice":"This feed contains at most 100 jobs (the most recently enriched). For the full corpus, use the paginated /stats/by-facet endpoint or /search.","x-generator":"yubhub-xml-generator","x-rights":"Free to redistribute with attribution: \"Data by YubHub (https://yubhub.co)\"","x-schema":"Each entry in `jobs` follows https://schema.org/JobPosting. YubHub-native raw fields carry `x-` prefix.","jobs":[{"@context":"https://schema.org","@type":"JobPosting","identifier":{"@type":"PropertyValue","name":"YubHub","value":"job_8ca21f98-841"},"title":"CRA II","description":"<p>Syneos Health is seeking a CRA II based in Korea. 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href=\"https://yubhub.co\">YubHub</a>.</p>","url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/KOR-Client/CRA-II-based-in-Korea_25114151-1","directApply":true,"hiringOrganization":{"@type":"Organization","name":"Syneos Health","sameAs":"http://www.syneoshealth.com","logo":"https://logos.yubhub.co/syneoshealth.com.png"},"x-apply-url":"https://syneoshealth.wd12.myworkdayjobs.com/en-US/Syneos_Health_External_Site/job/KOR-Client/CRA-II-based-in-Korea_25114151-1","x-work-arrangement":null,"x-experience-level":"senior","x-job-type":"full-time","x-salary-range":null,"x-skills-required":["Good Clinical Practice","ICH Guidelines","regulatory requirements","computer skills","communication skills","interpersonal 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compliance.</p>\n<p>Responsibilities:</p>\n<ul>\n<li>Perform site qualification, site initiation, interim monitoring, site management activities, and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP, and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance.</li>\n<li>Verify the process of obtaining informed consent has been adequately performed and documented for each subject/patient, as required/appropriate.</li>\n<li>Assess factors that might affect subject/patient&#39;s safety and clinical data integrity at an investigator/physician site.</li>\n<li>Per the Clinical Monitoring/Site Management Plan (CMP/SMP): Assess site processes, conduct Source Document Review of appropriate site source documents and medical records.</li>\n<li>Verify required clinical data entered in the case report form (CRF) is accurate and complete.</li>\n<li>Apply query resolution techniques remotely and on-site, and provide guidance to site staff as 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