{"id":63832,"date":"2026-08-10T11:14:13","date_gmt":"2026-08-10T04:14:13","guid":{"rendered":"https:\/\/www.oucru.org\/?post_type=career&#038;p=63832"},"modified":"2026-08-10T15:31:20","modified_gmt":"2026-08-10T08:31:20","slug":"oucru-id-site-study-nurse-keerom-papua","status":"publish","type":"career","link":"https:\/\/www.oucru.org\/id\/career\/oucru-id-site-study-nurse-keerom-papua\/","title":{"rendered":"OUCRU ID &#8211; Site Study Nurse &#8211; Keerom, Papua"},"content":{"rendered":"\n<ul class=\"wp-block-list\">\n<li><strong>Group:<\/strong>&nbsp;Clinical Research Management and Governance, OUCRU Indonesia<\/li>\n\n\n\n<li><strong>Location:<\/strong>&nbsp;Keerom, Papua<\/li>\n\n\n\n<li><strong>Hours of Work:<\/strong>&nbsp;1.0 FTE<\/li>\n\n\n\n<li><strong>Tenure:<\/strong>&nbsp;Initially for&nbsp;01&nbsp;years&nbsp;with&nbsp;possibility&nbsp;of extension<\/li>\n\n\n\n<li><strong>Reporting to: <\/strong>Senior Site Physician (with dotted line to Site Clinical Research Operations Manager)<\/li>\n\n\n\n<li><strong>Vacancy Reference:<\/strong>&nbsp;OUCRU ID &#8211; Site Study Nurse &#8211; Keerom, Papua<\/li>\n<\/ul>\n\n\n\n<p><\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Background<\/h3>\n\n\n\n<p id=\"p-rc_9c80046eb049ee0d-49\">The Oxford University Clinical Research Unit (OUCRU) is a large-scale clinical and public health research unit, with sites offices in Ho Chi Minh City and Hanoi in Vietnam, Jakarta in Indonesia and Kathmandu in Nepal. In Vietnam, we are hosted by the Hospital of Tropical Diseases (HTD) in Ho Chi Minh City, and the National Hospital for Tropical Diseases (NHTD) in Hanoi.\u00a0OUCRU Nepal closely collaborates with the National Academy of Medical Sciences in Kathmandu, and OUCRU Indonesia exists in partnership with the Universitas Indonesia. As a\u00a0Wellcome\u00a0Trust Africa Asia\u00a0Programme, we have received considerable support from the\u00a0Wellcome\u00a0Trust since our establishment in 1991.\u00a0\u00a0<\/p>\n\n\n\n<p>OUCRU\u2019s vision is to have&nbsp;local,&nbsp;regional&nbsp;and global impact on health by leading a locally driven research&nbsp;programme&nbsp;on infectious diseases in Southeast Asia. Priority is given to health issues important to the hospitals where we work, and to the countries&nbsp;as a whole where&nbsp;we&nbsp;operate: Vietnam,&nbsp;Indonesia&nbsp;and Nepal.&nbsp;&nbsp;All work is intended not only to&nbsp;benefit&nbsp;the patients seen daily at our host hospitals, but also to help improve patient care.&nbsp;<\/p>\n\n\n\n<p>Please see more information on OUCRU website:&nbsp;<a href=\"http:\/\/www.oucru.org\/\" target=\"_blank\" rel=\"noreferrer noopener\">www.oucru.org<\/a>&nbsp;<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Job Summary<\/h3>\n\n\n\n<p>Overall, the study nurse supports the day-to-day conduct of clinical research at the site level, ensuring studies are carried out according to protocol, ethical standards, and regulatory requirements.&nbsp;The nurse coordinates participant recruitment,&nbsp;may support the study physician in conducting informed consent, scheduling study visits, and perform data collection while&nbsp;maintaining&nbsp;accurate&nbsp;research documentation. They&nbsp;observe&nbsp;participant safety, administer study interventions when&nbsp;required, and communicate closely with investigators, sponsors, and multidisciplinary teams. Additionally, they help ensure compliance with Good Clinical Practice (GCP) and contribute to high-quality, reliable research outcomes.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Requirements<\/h3>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Medical nurse with demonstrable experience of at least 1-year duration in one or more of the job descriptions outlined above;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Has active Surat Tanda&nbsp;Registrasi&nbsp;(STR) Experience and Skills&nbsp;&nbsp;<\/li>\n\n\n\n<li>BLS and ACLS Certification are&nbsp;required;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Previous&nbsp;research experience is preferred;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Excellent written English and Bahasa Indonesia, with proven ability to research and write accessible;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Computer literacy and&nbsp;proficiency;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Excellent interpersonal&nbsp;skills;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Demonstrate&nbsp;a high level&nbsp;of&nbsp;organization&nbsp;skills and attention to details. Ability to manage and\/or supervise complex research endeavors;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Ability to work effectively as a team with healthcare personnel at all levels;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Evidence of self-motivation, initiative,&nbsp;creativity&nbsp;and attention to detail;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Demonstrate&nbsp;high level&nbsp;of organization skills and attention to details;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Ability to&nbsp;observe, comprehend,&nbsp;analyze&nbsp;and solve problems independently;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Recognize scope of decision making, with ability to receive directions as&nbsp;appropriate;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Willing to be&nbsp;located&nbsp;at trial site within required contract period&nbsp;&nbsp;<\/li>\n\n\n\n<li>Willing to work on shift&nbsp;<\/li>\n<\/ul>\n\n\n\n<h3 class=\"wp-block-heading\">Key Responsibilities<\/h3>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Involve in participant recruitment \u2013&nbsp;identify&nbsp;potential participants, approach potential study&nbsp;participants&nbsp;and provide information about the clinical research&nbsp;&nbsp;<\/li>\n\n\n\n<li>Carry out clinical activities as scheduled in the protocol, including but not limited to performing physical examination, checks vital signs and symptoms,&nbsp;collect&nbsp;samples and&nbsp;obtain&nbsp;medical information&nbsp;of&nbsp;the participant, in support of the Study Physician.&nbsp;<\/li>\n\n\n\n<li>Support the Study Physician in conducting screening on the potential participants, based on inclusion and exclusion criteria&nbsp;stated&nbsp;in the protocol.&nbsp;&nbsp;<\/li>\n\n\n\n<li>Observe&nbsp;participants following intervention to ensure any safety issue is managed promptly and accordingly&nbsp;<\/li>\n\n\n\n<li>Provide primary healthcare management or first aid to study participants experiencing AE\/SAE related to the study intervention&nbsp;&nbsp;<\/li>\n\n\n\n<li>Provide information and instruction to the participants on how to complete participant\u2019s diary, self-assessment&nbsp;and reporting in case of AE\/SAE, and how to contact study team&nbsp;&nbsp;<\/li>\n\n\n\n<li>Prepare&nbsp;participant&nbsp;for visit schedule &#8211; ensure the&nbsp;participant&nbsp;understand what the procedures he\/she will have for the visit\/s.&nbsp;&nbsp;<\/li>\n\n\n\n<li>Conduct follow up and ensure the completeness of the participant\u2019s data&nbsp;&nbsp;<\/li>\n\n\n\n<li>Ensure the sample collection is performed as scheduled in the approved protocol&nbsp;&nbsp;<\/li>\n\n\n\n<li>Enter participant data to the electronic Case Report Form (CRF), as assigned by the site investigator\/principal investigator, if&nbsp;required&nbsp;&nbsp;<\/li>\n\n\n\n<li>Support in resolving queries generated on the participant\u2019s data&nbsp;entered to&nbsp;the database in&nbsp;timely&nbsp;manner&nbsp;&nbsp;<\/li>\n\n\n\n<li>Ensure that the clinical research is conducted according to the protocol, Good Clinical Practice (ICH-GCP), Cara Uji Klinik yang Baik (CUKB) and all applicable regulations&nbsp;<\/li>\n\n\n\n<li>Act as a&nbsp;back up&nbsp;to the Site Pharmacist in managing investigational medicinal products (IMP),&nbsp;monitor&nbsp;storage and accountability at site, as applicable; or as assigned by the site investigator\/principal investigator&nbsp;<\/li>\n<\/ul>\n\n\n\n<h3 class=\"wp-block-heading\">How to Apply<\/h3>\n\n\n\n<p>Please submit the following documents by email to&nbsp;<strong>recruitment.id@oucru.org<\/strong>:<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Cover letter<\/li>\n\n\n\n<li>Curriculum vitae<\/li>\n\n\n\n<li>Names and contact details of a minimum of two professional referees<\/li>\n\n\n\n<li>Salary expectations<\/li>\n<\/ul>\n\n\n\n<blockquote class=\"wp-block-quote is-layout-flow wp-block-quote-is-layout-flow\">\n<p><strong>Email Subject:<\/strong>&nbsp;Please quote the reference&nbsp;\u201c<strong>OUCRU ID &#8211; Site Study Nurse &#8211; Keerom, Papua \u2013 Your name\u201d<\/strong>&nbsp;<\/p>\n<\/blockquote>\n\n\n\n<p><strong>Deadline for submission<\/strong>: 24 August 2026<\/p>\n\n\n\n<p><em>Only shortlisted candidates will be contacted.<\/em><\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Contact person<\/h3>\n\n\n\n<p>Iwan Tarmizi\/Eka Yuninda<\/p>\n\n\n\n<figure class=\"wp-block-image\"><a href=\"https:\/\/www.ui.ac.id\/\"><img decoding=\"async\" width=\"60\" height=\"60\" src=\"https:\/\/www.oucru.org\/wp-content\/uploads\/2022\/10\/ui-logo.png\" alt=\"\" class=\"wp-image-56140\" \/><\/a><\/figure>\n\n\n\n<p><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Background The Oxford University Clinical Research Unit (OUCRU) is a large-scale clinical and public health research unit, with sites offices in Ho Chi Minh City and Hanoi in Vietnam, Jakarta [&hellip;]<\/p>\n","protected":false},"author":55,"featured_media":0,"menu_order":0,"template":"","meta":{"_acf_changed":false,"_links_to":"","_links_to_target":""},"categories":[146],"tags":[],"class_list":["post-63832","career","type-career","status-publish","hentry","category-indonesia"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v25.3.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>OUCRU ID - Site Study Nurse - Keerom, Papua - OUCRU<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.oucru.org\/id\/career\/oucru-id-site-study-nurse-keerom-papua\/\" \/>\n<meta property=\"og:locale\" content=\"id_ID\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"OUCRU ID - Site Study Nurse - Keerom, Papua - OUCRU\" \/>\n<meta property=\"og:description\" content=\"Background The Oxford 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