{"id":4280,"date":"2023-05-23T11:53:24","date_gmt":"2023-05-23T03:53:24","guid":{"rendered":"https:\/\/credevo.com\/s\/?page_id=4280"},"modified":"2023-05-23T11:55:28","modified_gmt":"2023-05-23T03:55:28","slug":"clinical-trials-specialist","status":"publish","type":"page","link":"https:\/\/credevo.com\/s\/clinical-trials-specialist\/","title":{"rendered":"Clinical Trials Specialist"},"content":{"rendered":"\n<h3 class=\"wp-block-heading\">Job Description<\/h3>\n\n\n\n<figure class=\"wp-block-table\"><table><tbody><tr><td><strong>Job Title<\/strong><\/td><td>Clinical Trials Specialist<\/td><\/tr><tr><td><strong>Reports to<\/strong><\/td><td>CEO<\/td><\/tr><tr><td><strong>Department<\/strong><\/td><td>Clinical Trials<\/td><\/tr><tr><td><strong>Location<\/strong><\/td><td>Remote<\/td><\/tr><tr><td><strong>Job Type<\/strong><\/td><td>Contract<\/td><\/tr><tr><td><strong>Supervises&nbsp;<\/strong><\/td><td>None<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<h3 class=\"wp-block-heading\">Company Overview<\/h3>\n\n\n\n<p><a href=\"https:\/\/credevo.com\" target=\"_blank\" rel=\"noreferrer noopener\"><strong>Credevo<\/strong><\/a> is a global consulting organization supporting healthcare product development from clinical development to commercialization. Credevo provides strategic support in areas such as regulatory, clinical development, licensing (out-\/in-), and feasibility support, for products including pharmaceuticals, biologics, nutraceuticals, and medical devices.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Position Overview <\/h3>\n\n\n\n<p>We are seeking a highly motivated and detail-oriented individual to join our team as a Clinical Trials Specialist. In this role, you will be responsible for providing strategic support and coordination for the successful planning and execution of clinical trials.<\/p>\n\n\n\n<p>This position is open to candidates from India, the Philippines, Thailand, Malaysia, Sri Lanka, and Indonesia.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Essential duties and responsibilities (including, but not limited to the following):<\/h3>\n\n\n\n<p>The incumbent should be able to perform the following activities while working remotely:<\/p>\n\n\n\n<ul class=\"wp-block-list\"><li>Communication and coordination with customers to understand their needs for clinical trials.<\/li><li>Evaluation of product details, business needs, and customer requirements to&nbsp;<ul><li>identify the study rationale,<\/li><li>identify key geographic regions for the trial,<\/li><li>prepare a strategic plan for the trial and <\/li><li>advise on the way forward.<\/li><\/ul><\/li><li>Provide on-hand support in the identification, selection, and management of key internal and external teams for various activities in the clinical trial.<\/li><li>Collaborate with relevant team members to develop and implement study protocols, standard operating procedures (SOPs), and informed consent documents.<\/li><li>Assist in the selection and evaluation of investigational sites, investigators, and vendors, ensuring their compliance with study requirements.<\/li><li>Achieve study objectives and timelines by coordinating with relevant teams for the preparation and submission of applications for regulatory and ethics committee approvals<\/li><li>Collection, maintenance, and review of study documents, including case report forms (CRFs), source documentation, and regulatory files.<\/li><li>Effective clinical operations, viz. monitoring and tracking study progress, including enrollment status, adverse events, and protocol deviations<\/li><li>The timely and accurate completion of data entry and data management activities, including data cleaning, query resolution, and database lock<\/li><li>Ensuring timely reporting to the management team and relevant stakeholders<\/li><li>Maintain comprehensive and up-to-date knowledge of relevant regulations, guidelines, and best practices in clinical research.<\/li><li>Contribute to the development and improvement of study processes, SOPs, and quality control measures.<\/li><\/ul>\n\n\n\n<h3 class=\"wp-block-heading\">Job Requirements<\/h3>\n\n\n\n<ol class=\"wp-block-list\"><li><strong>Education: <\/strong>At least a Masters&#8217;s degree in medicine, pharmacy, or a scientific- or healthcare-related field.<\/li><li><strong>Prior Work Experience: <\/strong>At least 5 years of experience in clinical trials, preferably focusing on clinical trial strategy, plan, and design.<\/li><li><strong>Job Knowledge:<\/strong><ul><li>Strong understanding of Good Clinical Practice (GCP) guidelines, industry standards, and regulatory requirements, particularly in regions of Southeast Asia, East Asia, Japan, and Australia<\/li><li>Strong understanding of drug development process and clinical trial methodology &amp; operations.<\/li><li>Excellent attention to detail and the ability to prioritize and multitask in a fast-paced environment.<\/li><li>Strong written and verbal communication skills, with the ability to effectively collaborate with internal and external stakeholders.<\/li><li>Demonstrable problem-solving skills and ability to exercise independent judgment.<\/li><li>Proficiency in using clinical trial management systems and electronic data capture (EDC) systems.<\/li><li>Advanced level expertise in using Excel and Word.<\/li><li>On-hands past experience of conducting studies in South East Asia, East Asia, Japan, and Australia (desirable).<\/li><li>Certification in clinical research\/project management (such as ACRP or SoCRA or PMP) (desirable).<\/li><\/ul><\/li><li><strong>Language Proficiency: <\/strong>Expert written communication skills in the English language &#8211; This should be demonstrated by prior work and during the selection process. Good English speaking skills with the ability to understand different international accents are also required.\u00a0<\/li><\/ol>\n\n\n\n<div class=\"wp-block-buttons is-content-justification-center is-layout-flex wp-block-buttons-is-layout-flex\">\n<div class=\"wp-block-button\"><a class=\"wp-block-button__link has-background\" href=\"https:\/\/forms.gle\/QfBgeAyvd3ywEYYj9\" style=\"background-color:#0099e5\" target=\"_blank\" rel=\"noreferrer noopener\">Apply Using Gmail \/ Google Account<\/a><\/div>\n<\/div>\n\n\n\n<p class=\"has-text-align-center has-small-font-size\"><strong><em>IMPORTANT:<\/em><\/strong><em style=\"font-weight: bold;\"> You will need to login to your gmail \/ google account for authentication to apply.<\/em><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Job Description Job Title Clinical Trials Specialist Reports to CEO Department Clinical Trials Location Remote Job Type Contract Supervises&nbsp; None Company Overview Credevo is a global consulting organization supporting healthcare product development from clinical development to commercialization. Credevo provides strategic support in areas such as regulatory, clinical development, licensing (out-\/in-), and feasibility support, for products [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_acf_changed":false,"footnotes":""},"class_list":["post-4280","page","type-page","status-publish","hentry"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v25.3.1 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Clinical Trials Specialist - Credevo<\/title>\n<meta name=\"description\" content=\"We are seeking a highly motivated and detail-oriented individual to join our team as a Clinical Trials Specialist.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/credevo.com\/s\/clinical-trials-specialist\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Clinical Trials Specialist - Credevo\" \/>\n<meta property=\"og:description\" content=\"We are seeking a highly motivated and detail-oriented individual to join our team as a Clinical Trials Specialist.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/credevo.com\/s\/clinical-trials-specialist\/\" \/>\n<meta property=\"og:site_name\" content=\"Credevo\" \/>\n<meta property=\"article:publisher\" content=\"https:\/\/www.facebook.com\/credevo\" \/>\n<meta property=\"article:modified_time\" content=\"2023-05-23T03:55:28+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:site\" content=\"@gocredevo\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"3 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/credevo.com\/s\/clinical-trials-specialist\/\",\"url\":\"https:\/\/credevo.com\/s\/clinical-trials-specialist\/\",\"name\":\"Clinical Trials Specialist - Credevo\",\"isPartOf\":{\"@id\":\"https:\/\/credevo.com\/s\/#website\"},\"datePublished\":\"2023-05-23T03:53:24+00:00\",\"dateModified\":\"2023-05-23T03:55:28+00:00\",\"description\":\"We are seeking a highly motivated and detail-oriented individual to join our team as a Clinical Trials Specialist.\",\"breadcrumb\":{\"@id\":\"https:\/\/credevo.com\/s\/clinical-trials-specialist\/#breadcrumb\"},\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/credevo.com\/s\/clinical-trials-specialist\/\"]}]},{\"@type\":\"BreadcrumbList\",\"@id\":\"https:\/\/credevo.com\/s\/clinical-trials-specialist\/#breadcrumb\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Services\",\"item\":\"https:\/\/credevo.com\/s\/\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Clinical Trials Specialist\"}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/credevo.com\/s\/#website\",\"url\":\"https:\/\/credevo.com\/s\/\",\"name\":\"Credevo\",\"description\":\"Healthcare Product Development from Clinical Development to Commercialization\",\"publisher\":{\"@id\":\"https:\/\/credevo.com\/s\/#organization\"},\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/credevo.com\/s\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"},{\"@type\":\"Organization\",\"@id\":\"https:\/\/credevo.com\/s\/#organization\",\"name\":\"Credevo Pte. 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