{"id":63834,"date":"2026-08-10T12:05:05","date_gmt":"2026-08-10T05:05:05","guid":{"rendered":"https:\/\/www.oucru.org\/?post_type=career&#038;p=63834"},"modified":"2026-08-10T15:31:26","modified_gmt":"2026-08-10T08:31:26","slug":"oucru-id-site-clinical-trial-pharmacist-keerom-papua","status":"publish","type":"career","link":"https:\/\/www.oucru.org\/vi\/career\/oucru-id-site-clinical-trial-pharmacist-keerom-papua\/","title":{"rendered":"OUCRU ID \u2013 Site Clinical Trial Pharmacist\u00a0 \u2013 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>Site Clinical Operations Manager (with dotted line to Clinical Trial Pharmacist)<\/li>\n\n\n\n<li><strong>Vacancy Reference:<\/strong>&nbsp;OUCRU ID \u2013 Site Clinical Trial Pharmacist \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.\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\">Requirements<\/h3>\n\n\n\n<p><strong>Qualifications<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Registered pharmacist in Indonesia <\/li>\n\n\n\n<li>Experience in managing investigational medicinal drug in clinical trials and\/or as hospital pharmacist is preferred <\/li>\n\n\n\n<li>Willing to be located at trial site within required contract period<\/li>\n<\/ul>\n\n\n\n<p><strong>Knowledge &amp; Skills<\/strong><\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>English and Bahasa Indonesia (Fluent\/Native) <\/li>\n\n\n\n<li>Clinical trials conduct <\/li>\n\n\n\n<li>Clinical Trial Guidelines (Local &amp; International)<\/li>\n\n\n\n<li>Good Manufacturing Practice (GMP) and applicable local &amp; international guidance<\/li>\n\n\n\n<li>Good Distribution Practice (GDP)<\/li>\n\n\n\n<li>Quality Assurance (QA) <\/li>\n\n\n\n<li>Process development <\/li>\n\n\n\n<li>Communication <\/li>\n\n\n\n<li>Interpersonal skills <\/li>\n\n\n\n<li>Documentation and archiving<\/li>\n<\/ul>\n\n\n\n<h3 class=\"wp-block-heading\">Key Responsibilities<\/h3>\n\n\n\n<p><strong>Investigational Drug Management<\/strong>&nbsp;<\/p>\n\n\n\n<ul class=\"wp-block-list\">\n<li>Reviews protocols and study documents related to investigational drug management;&nbsp;<\/li>\n\n\n\n<li>Liaise with study team and\/or coordinator to&nbsp;establish&nbsp;site pharmacy\u2019s role, and to implement dispensing,&nbsp;compounding&nbsp;and billing procedures;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Communicates with, and trains study staff in any aspect of the clinical investigational drug trial.&nbsp;&nbsp;<\/li>\n\n\n\n<li>Responsible for pharmacy binder which&nbsp;contains&nbsp;a study summary, protocol, dispensing procedures, completed samples of required paperwork, dispensing checklist, fee schedule, and investigational drug-related billing procedures;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Ensures and coordinates distribution of an up-to-date investigational drug trials list and stock at OUCRU ID;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Reviews and ensures that the SOPs and procedures related to investigational drug are implemented&nbsp;in accordance with&nbsp;the applicable requirements and protocol;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Ensures that the investigational drug is handled, stored,&nbsp;identified&nbsp;and dispensed&nbsp;in accordance with&nbsp;the applicable requirements and quality standards;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Ensures the accountability through good documentation practice in all activities related to investigational drug management;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Liaise with the hospital and\/or health facility pharmacy involved in storage and distribution of investigational drug;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Perform randomization in drugs distribution to subjects;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Provide the trial subject the correct information on administration and storage&nbsp;in accordance with&nbsp;the protocol;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Manage IMP related vendors\/service providers in liaison with Procurement\/Operations Team, conduct audit\/assessments&nbsp;and ensure compliance to relevant regulations and requirements;&nbsp;&nbsp;<\/li>\n\n\n\n<li>In liaison with Research Regulatory team, prepare IMP-related documents&nbsp;required&nbsp;for clinical trial submission;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Manage IMP quality issues in collaboration with relevant study team;&nbsp;<\/li>\n\n\n\n<li>Provides input in terms of administrative aspects of clinical trial to the study team to ensure compliance with the applicable regulations,&nbsp;requirements&nbsp;and standards;&nbsp;&nbsp;<\/li>\n\n\n\n<li>Performs other tasks as assigned by the supervisor&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 \u2013 Site Clinical Trial Pharmacist \u2013 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 class=\"glg-a-custom-wrap\" 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-63834","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 \u2013 Site Clinical Trial Pharmacist\u00a0 \u2013 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\/vi\/career\/oucru-id-site-clinical-trial-pharmacist-keerom-papua\/\" \/>\n<meta property=\"og:locale\" content=\"vi_VN\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"OUCRU ID \u2013 Site Clinical Trial Pharmacist\u00a0 \u2013 Keerom, Papua - 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