{"id":66292,"date":"2026-09-11T16:13:41","date_gmt":"2026-09-11T09:13:41","guid":{"rendered":"https:\/\/www.oucru.org\/?post_type=career&#038;p=66292"},"modified":"2026-09-11T16:13:48","modified_gmt":"2026-09-11T09:13:48","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 \u2013 Site Study Nurse\u00a0 \u2013 Keerom, Papua"},"content":{"rendered":"\n<ul class=\"wp-block-list\">\n<li><strong>Group:<\/strong>\u00a0Clinical Research Management and Governance, OUCRU Indonesia<\/li>\n\n\n\n<li><strong>Location:<\/strong>\u00a0Keerom, Papua<\/li>\n\n\n\n<li><strong>Hours of Work:<\/strong>\u00a01.0 FTE<\/li>\n\n\n\n<li><strong>Tenure:<\/strong>\u00a0Initially for\u00a001\u00a0years\u00a0with\u00a0possibility\u00a0of extension<\/li>\n\n\n\n<li><strong>Reporting to:\u00a0<\/strong>Senior Site Physician (with dotted line to Site Clinical Research Operations Manager)<\/li>\n\n\n\n<li><strong>Vacancy Reference:<\/strong>\u00a0OUCRU ID \u2013 Site Study Nurse \u2013 Keerom, Papua<\/li>\n<\/ul>\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.&nbsp;OUCRU Nepal closely collaborates with the National Academy of Medical Sciences in Kathmandu, and OUCRU Indonesia exists in partnership with the Universitas Indonesia. As a&nbsp;Wellcome&nbsp;Trust Africa Asia&nbsp;Programme, we have received considerable support from the&nbsp;Wellcome&nbsp;Trust since our establishment in 1991.&nbsp;&nbsp;<\/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\">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;<\/li>\n\n\n\n<li>Has active Surat Tanda Registrasi (STR)<\/li>\n\n\n\n<li>BLS and ACLS Certification are required;<\/li>\n\n\n\n<li>Previous research experience is preferred;<\/li>\n\n\n\n<li>Excellent written English and Bahasa Indonesia, with proven ability to research and write<br>accessible;<\/li>\n\n\n\n<li>Computer literacy and proficiency;<\/li>\n\n\n\n<li>Excellent interpersonal skills;<\/li>\n\n\n\n<li>Demonstrate a high level of organization skills and attention to details. Ability to manage<br>and\/or supervise complex research endeavors;<\/li>\n\n\n\n<li>Ability to work effectively as a team with healthcare personnel at all levels;<\/li>\n\n\n\n<li>Evidence of self-motivation, initiative, creativity and attention to detail;<\/li>\n\n\n\n<li>Demonstrate high level of organization skills and attention to details;<\/li>\n\n\n\n<li>Ability to observe, comprehend, analyze and solve problems independently;<\/li>\n\n\n\n<li>Recognize scope of decision making, with ability to receive directions as appropriate;<\/li>\n\n\n\n<li>Willing to be located at trial site within required contract period<\/li>\n\n\n\n<li>Willing to work on shift<\/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 identify potential participants, approach potential study participants and provide information about the clinical research<\/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, collect samples and obtain medical information of the participant, in support of the Study Physician.<\/li>\n\n\n\n<li>Support the Study Physician in conducting screening on the potential participants, based on inclusion and exclusion criteria stated in the protocol.<\/li>\n\n\n\n<li>Observe participants following intervention to ensure any safety issue is managed promptly and accordingly<\/li>\n\n\n\n<li>Provide primary healthcare management or first aid to study participants experiencing AE\/SAE related to the study intervention<\/li>\n\n\n\n<li>Provide information and instruction to the participants on how to complete participant\u2019s diary, self-assessment and reporting in case of AE\/SAE, and how to contact study team<\/li>\n\n\n\n<li>Prepare participant for visit schedule &#8211; ensure the participant understand what the procedures he\/she will have for the visit\/s.<\/li>\n\n\n\n<li>Conduct follow up and ensure the completeness of the participant\u2019s data <\/li>\n\n\n\n<li>Ensure the sample collection is performed as scheduled in the approved protocol<\/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 required<\/li>\n\n\n\n<li>Support in resolving queries generated on the participant\u2019s data entered to the database in timely manner<\/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<\/li>\n\n\n\n<li>Act as a back up to the Site Pharmacist in managing investigational medicinal products (IMP), monitor storage and accountability at site, as applicable; or as assigned by the site investigator\/principal investigator<\/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>\u00a0Please quote the reference\u00a0\u201c<strong>OUCRU ID \u2013 Site Study Nurse \u2013 Keerom, Papua \u2013 Your name\u201d<\/strong>\u00a0<\/p>\n<\/blockquote>\n\n\n\n<p><strong>Deadline for submission<\/strong>: 18 September 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<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-66292","career","type-career","status-publish","hentry","category-indonesia"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v25.3.1 - 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