{"id":9326,"date":"2025-09-15T08:23:48","date_gmt":"2025-09-15T02:53:48","guid":{"rendered":"https:\/\/pharmaceuticalcarrier.com\/?post_type=job_listing&#038;p=9326"},"modified":"2025-09-15T08:23:51","modified_gmt":"2025-09-15T02:53:51","slug":"clinical-document-author-virtusa-bengaluru-gurugram-hybrid-contract-role","status":"publish","type":"job_listing","link":"https:\/\/pharmaceuticalcarrier.com\/index.php\/job\/clinical-document-author-virtusa-bengaluru-gurugram-hybrid-contract-role\/","title":{"rendered":"Clinical Document Author \u2013 Virtusa (Bengaluru &amp; Gurugram | Hybrid, Contract Role)"},"content":{"rendered":"<h2 data-start=\"213\" data-end=\"235\"><strong data-start=\"216\" data-end=\"233\">About Virtusa<\/strong><\/h2>\n<p data-start=\"236\" data-end=\"634\">Virtusa is a <strong data-start=\"249\" data-end=\"305\">global leader in IT and digital engineering services<\/strong>, partnering with top pharmaceutical and biotech companies to deliver transformative solutions. We are currently hiring <strong data-start=\"425\" data-end=\"454\">Clinical Document Authors<\/strong> for our teams in <strong data-start=\"472\" data-end=\"498\">Bengaluru and Gurugram<\/strong>. This <strong data-start=\"505\" data-end=\"536\">hybrid, contract-based role<\/strong> is perfect for professionals eager to shape high-quality regulatory and clinical documentation.<\/p><div class=\"pharm-content\" id=\"pharm-1924533408\"><script async src=\"\/\/pagead2.googlesyndication.com\/pagead\/js\/adsbygoogle.js?client=ca-pub-8402705006112223\" crossorigin=\"anonymous\"><\/script><ins class=\"adsbygoogle\" style=\"display:block;\" data-ad-client=\"ca-pub-8402705006112223\" \ndata-ad-slot=\"7652789694\" \ndata-ad-format=\"auto\"><\/ins>\n<script> \n(adsbygoogle = window.adsbygoogle || []).push({}); \n<\/script>\n<\/div>\n<hr data-start=\"636\" data-end=\"639\" \/>\n<h2 data-start=\"641\" data-end=\"670\"><strong data-start=\"644\" data-end=\"668\">Key Responsibilities<\/strong><\/h2>\n<p data-start=\"671\" data-end=\"713\">As a Clinical Document Author, you will:<\/p>\n<ul data-start=\"714\" data-end=\"1372\">\n<li data-start=\"714\" data-end=\"867\">\n<p data-start=\"716\" data-end=\"867\">Draft and review clinical trial documents including <strong data-start=\"768\" data-end=\"864\">Protocols, Informed Consent Forms (ICFs), Clinical Study Reports (CSRs), and Summary Reports<\/strong>.<\/p>\n<\/li>\n<li data-start=\"868\" data-end=\"944\">\n<p data-start=\"870\" data-end=\"944\">Leverage AI-assisted tools to optimize document drafting and efficiency.<\/p>\n<\/li>\n<li data-start=\"945\" data-end=\"1041\">\n<p data-start=\"947\" data-end=\"1041\">Apply knowledge of <strong data-start=\"966\" data-end=\"1028\">clinical trial phases, study designs, and drug development<\/strong> processes.<\/p>\n<\/li>\n<li data-start=\"1042\" data-end=\"1105\">\n<p data-start=\"1044\" data-end=\"1105\">Ensure compliance with <strong data-start=\"1067\" data-end=\"1092\">FDA, EMA, and ICH-GCP<\/strong> standards.<\/p>\n<\/li>\n<li data-start=\"1106\" data-end=\"1188\">\n<p data-start=\"1108\" data-end=\"1188\">Use <strong data-start=\"1112\" data-end=\"1152\">medical terminologies and ontologies<\/strong> to maintain clarity and accuracy.<\/p>\n<\/li>\n<li data-start=\"1189\" data-end=\"1259\">\n<p data-start=\"1191\" data-end=\"1259\">Conduct quality checks, ensuring timely delivery of documentation.<\/p>\n<\/li>\n<li data-start=\"1260\" data-end=\"1372\">\n<p data-start=\"1262\" data-end=\"1372\">Collaborate with cross-functional teams and project managers, identifying and escalating risks where needed.<\/p>\n<\/li>\n<\/ul>\n<hr data-start=\"1374\" data-end=\"1377\" \/>\n<h2 data-start=\"1379\" data-end=\"1402\"><strong data-start=\"1382\" data-end=\"1400\">Qualifications<\/strong><\/h2>\n<ul data-start=\"1403\" data-end=\"1770\">\n<li data-start=\"1403\" data-end=\"1475\">\n<p data-start=\"1405\" data-end=\"1475\"><strong data-start=\"1405\" data-end=\"1419\">Education:<\/strong> Graduate in any discipline (Life Sciences preferred).<\/p>\n<\/li>\n<li data-start=\"1476\" data-end=\"1576\">\n<p data-start=\"1478\" data-end=\"1576\"><strong data-start=\"1478\" data-end=\"1493\">Experience:<\/strong> 1\u20135 years in <strong data-start=\"1507\" data-end=\"1573\">clinical documentation, regulatory writing, or medical writing<\/strong>.<\/p>\n<\/li>\n<li data-start=\"1577\" data-end=\"1675\">\n<p data-start=\"1579\" data-end=\"1675\"><strong data-start=\"1579\" data-end=\"1590\">Skills:<\/strong> Familiarity with <strong data-start=\"1608\" data-end=\"1650\">protocols, ICFs, ICH-GCP, FDA, and EMA<\/strong> regulatory frameworks.<\/p>\n<\/li>\n<li data-start=\"1676\" data-end=\"1720\">\n<p data-start=\"1678\" data-end=\"1720\"><strong data-start=\"1678\" data-end=\"1696\">Notice Period:<\/strong> Immediate to 15 days.<\/p>\n<\/li>\n<li data-start=\"1721\" data-end=\"1770\">\n<p data-start=\"1723\" data-end=\"1770\"><strong data-start=\"1723\" data-end=\"1736\">Location:<\/strong> Bengaluru or Gurugram (Hybrid).<\/p>\n<\/li>\n<\/ul>\n<hr data-start=\"1772\" data-end=\"1775\" \/>\n<h2 data-start=\"1777\" data-end=\"1803\"><strong data-start=\"1780\" data-end=\"1801\">Why Join Virtusa?<\/strong><\/h2>\n<ul data-start=\"1804\" data-end=\"2069\">\n<li data-start=\"1804\" data-end=\"1879\">\n<p data-start=\"1806\" data-end=\"1879\">Opportunity to <strong data-start=\"1821\" data-end=\"1876\">work with global pharmaceutical and biotech leaders<\/strong>.<\/p>\n<\/li>\n<li data-start=\"1880\" data-end=\"1972\">\n<p data-start=\"1882\" data-end=\"1972\">Gain hands-on experience in <strong data-start=\"1910\" data-end=\"1969\">regulatory documentation and AI-powered authoring tools<\/strong>.<\/p>\n<\/li>\n<li data-start=\"1973\" data-end=\"2019\">\n<p data-start=\"1975\" data-end=\"2019\">Collaborative and innovative work culture.<\/p>\n<\/li>\n<li data-start=\"2020\" data-end=\"2069\">\n<p data-start=\"2022\" data-end=\"2069\">Hybrid working model with contract stability.<\/p>\n<\/li>\n<\/ul>\n<hr data-start=\"2071\" data-end=\"2074\" \/>\n<h2 data-start=\"2076\" data-end=\"2097\"><strong data-start=\"2079\" data-end=\"2095\">How to Apply<\/strong><\/h2>\n<p data-start=\"2098\" data-end=\"2238\">If you\u2019re ready to advance your career in <strong data-start=\"2140\" data-end=\"2175\">clinical and regulatory writing<\/strong>, send your updated CV to:<br data-start=\"2201\" data-end=\"2204\" \/>\ud83d\udce7 <strong data-start=\"2207\" data-end=\"2236\"><a class=\"decorated-link cursor-pointer\" rel=\"noopener\" data-start=\"2209\" data-end=\"2234\">sushma.n@people-prime.com<\/a><\/strong><\/p>\n<hr data-start=\"2240\" data-end=\"2243\" \/>\n<div class=\"col-lg-9 col-md-9 col-xs-12\">\n<div id=\"post-9322\" class=\"blog-post post-9322 job_listing type-job_listing status-publish has-post-thumbnail hentry job-type-full-time\">\n<div class=\"blog-post-text\">\n<div class=\"single_job_listing\">\n<div class=\"job_description\">\n<div class=\"flex flex-grow flex-col max-w-full\">\n<div class=\"min-h-[20px] text-message flex flex-col items-start whitespace-pre-wrap break-words [.text-message+&amp;]:mt-5 juice:w-full juice:items-end overflow-x-auto gap-2\" dir=\"auto\" data-message-author-role=\"assistant\" data-message-id=\"30431974-1fbd-432c-bfb7-d714d069d24b\">\n<div class=\"flex w-full flex-col gap-1 juice:empty:hidden juice:first:pt-[3px]\">\n<div class=\"markdown prose w-full break-words dark:prose-invert dark\">\n<p>For more articles,\u00a0<strong><a href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/ayurveda\/\">Kindly Click<\/a>\u00a0here<\/strong>.<\/p>\n<p>For pharmaceutical\u00a0<a title=\"jobs\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/jobs\/\">jobs<\/a>, follow us on<strong>\u00a0<a href=\"https:\/\/www.linkedin.com\/company\/pharmaceuticalcarrier\/?viewAsMember=true\" target=\"_blank\" rel=\"noopener\">LinkedIn<\/a><\/strong><\/p>\n<div class=\"job_description\">\n<p><strong>For more\u00a0<a title=\"jobs\" href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/jobs\/\">jobs<\/a>, kindly visit our job section.<\/strong><\/p>\n<p><a href=\"https:\/\/pharmaceuticalcarrier.com\/index.php\/jobs\/\">www.pharmaceuticalcarrier.com\/Jobs<\/a><\/p>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n<\/div>\n","protected":false},"author":1,"featured_media":9327,"template":"","meta":{"_uag_custom_page_level_css":"","_promoted":"","_job_location":"Bengaluru\/Gurugram, 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Virtusa Virtusa is a global leader in IT and digital engineering services, partnering with top pharmaceutical and biotech companies to deliver transformative solutions. We are currently hiring Clinical Document Authors for our teams in Bengaluru and Gurugram. This hybrid, Read More","_links":{"self":[{"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/job-listings\/9326","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/job-listings"}],"about":[{"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/types\/job_listing"}],"author":[{"embeddable":true,"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/users\/1"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/media\/9327"}],"wp:attachment":[{"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/media?parent=9326"}],"wp:term":[{"taxonomy":"job_listing_category","embeddable":true,"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/job-categories?post=9326"},{"taxonomy":"job_listing_type","embeddable":true,"href":"https:\/\/pharmaceuticalcarrier.com\/index.php\/wp-json\/wp\/v2\/job-types?post=9326"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}