{"id":6450,"date":"2026-07-12T20:12:12","date_gmt":"2026-07-12T20:12:12","guid":{"rendered":"https:\/\/globalpharmajobs.org\/?job_listing=accenture-hiring-clinical-data-sas-regulatory-affairs-pharmacovigilance-professionals"},"modified":"2026-07-12T20:12:12","modified_gmt":"2026-07-12T20:12:12","slug":"accenture-hiring-clinical-data-sas-regulatory-affairs-pharmacovigilance-professionals","status":"publish","type":"job_listing","link":"https:\/\/globalpharmajobs.org\/?job_listing=accenture-hiring-clinical-data-sas-regulatory-affairs-pharmacovigilance-professionals","title":{"rendered":"Accenture Hiring Clinical Data (SAS), Regulatory Affairs &#038; Pharmacovigilance Professionals"},"content":{"rendered":"<p><br \/>\n<\/p>\n<div>\n<p>\n\ud83d\udce2 Latest Clinical Data, Regulatory &amp; Pharmacovigilance Jobs\n<\/p>\n<p><a rel=\"nofollow\" target=\"_blank\" class=\"top-btn\" href=\"https:\/\/whatsapp.com\/channel\/0029VbAlflF4SpkDUPkczh1f\" style=\"background: 0% 0% repeat rgb(37, 211, 102); color: white;\"><br \/>\n\ud83d\udcf2 Join WhatsApp Channel<br \/>\n<\/a><\/p>\n<p><a rel=\"nofollow\" target=\"_blank\" class=\"top-btn\" href=\"https:\/\/t.me\/medicaljobshitechplus\" style=\"background: 0% 0% repeat rgb(0, 136, 204); color: white;\"><br \/>\n\ud83d\udce2 Join Telegram Channel<br \/>\n<\/a><\/p>\n<p><a rel=\"nofollow\" target=\"_blank\" class=\"top-btn\" href=\"https:\/\/www.linkedin.com\/company\/medical-jobs-hitechplus\/\" style=\"background: 0% 0% repeat rgb(0, 119, 181); color: white;\"><br \/>\n\ud83d\udcbc Follow on LinkedIn<\/a>n\u00a0<\/p>\n<div class=\"separator\" style=\"clear: both; text-align: center;\"><a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/blogger.googleusercontent.com\/img\/b\/R29vZ2xl\/AVvXsEj8cixj5fRztlmjN7Y-PBRjacSbDWeYPx6DYDsEPDnbtcJgZ1-Da2wGqcsKFw_b87I-BUfQU4E_WNFIHg4mdibvI8mBX18mrN0Hl0VfcilQ8Av7J0QriGn8aYk4ARDmipmHolSrxu1Mvb47DfK40ecRwiQgjFMbK6i7LhMcV44DIcrCHP7HirXdnCxj3bhA\/s1075\/IMG_2820.jpeg\" imageanchor=\"1\" style=\"margin-left: 1em; margin-right: 1em;\"><img decoding=\"async\" alt=\"Clinical Data, Regulatory &amp; Pharmacovigilance  Accenture B.Pharm, M.Pharm, BE, MSc Bengaluru &amp; Mumbai 1 - 5 Years\" border=\"0\" data-original-height=\"716\" data-original-width=\"1075\" src=\"https:\/\/blogger.googleusercontent.com\/img\/b\/R29vZ2xl\/AVvXsEj8cixj5fRztlmjN7Y-PBRjacSbDWeYPx6DYDsEPDnbtcJgZ1-Da2wGqcsKFw_b87I-BUfQU4E_WNFIHg4mdibvI8mBX18mrN0Hl0VfcilQ8Av7J0QriGn8aYk4ARDmipmHolSrxu1Mvb47DfK40ecRwiQgjFMbK6i7LhMcV44DIcrCHP7HirXdnCxj3bhA\/s16000\/IMG_2820.jpeg\" title=\"Clinical Data, Regulatory &amp; Pharmacovigilance  Accenture B.Pharm, M.Pharm, BE, MSc Bengaluru &amp; Mumbai 1 - 5 Years\"\/><\/a><\/div>\n<p>\n<span class=\"tag\">\u2714 Verified by Medical Jobs India<\/span>\n<\/p>\n<h2 class=\"title\">\nAccenture Hiring Clinical Data (SAS), Regulatory &amp; Pharmacovigilance Professionals<br \/>\n<\/h2>\n<div class=\"pill-group\">\n<p>\ud83c\udfe2 Accenture<\/p>\n<p>\ud83d\udccd Bengaluru &amp; Mumbai<\/p>\n<p>\ud83e\uddea Clinical Data &amp; PV<\/p>\n<p>\ud83d\udcc2 Regulatory Operations<\/p>\n<p>\ud83c\udf93 1\u20135 Years<\/p>\n<\/div>\n<p>\n<span class=\"highlight\">Accenture is hiring for multiple Life Sciences and Healthcare roles<\/span> across Clinical Data Services, Regulatory Operations, and Pharmacovigilance departments in India.\n<\/p>\n<p>\nThese opportunities are ideal for candidates interested in <b>Clinical Data Management, SAS Clinical, Regulatory Affairs, Pharmacovigilance, Safety Writing, Drug Safety Operations, and Global Healthcare Projects.<\/b>\n<\/p>\n<p><!--OVERVIEW--><\/p>\n<div class=\"card\">\n<h3>\ud83d\udccb Accenture Life Sciences Hiring Overview<\/h3>\n<ul>\n<li><b>Company:<\/b> Accenture<\/li>\n<li><b>Locations:<\/b> Mumbai &amp; Bengaluru<\/li>\n<li><b>Industry:<\/b> Life Sciences \/ Healthcare \/ Clinical Research<\/li>\n<li><b>Job Type:<\/b> Full-Time<\/li>\n<li><b>Qualification:<\/b> B.Pharm \/ M.Pharm \/ BE \/ MSc<\/li>\n<li><b>Experience:<\/b> 1\u20135 Years<\/li>\n<\/ul>\n<p>\n\ud83d\udcb0 <b>Expected Salary Range:<\/b> \u20b95 \u2013 \u20b912 LPA\n<\/p>\n<\/div>\n<p><!--ABOUT--><\/p>\n<div class=\"card\">\n<h3>\ud83c\udfe2 About Accenture<\/h3>\n<p>\nAccenture is a global professional services company specializing in digital, cloud, AI, consulting, technology, and operations across more than 120 countries.\n<\/p>\n<p>\nThe company\u2019s Life Sciences R&amp;D division supports pharmaceutical and biotechnology organizations in Clinical Trials, Pharmacovigilance, Regulatory Affairs, Clinical Data Management, and Drug Safety Operations.\n<\/p>\n<\/div>\n<p><!--CLINICAL DATA--><\/p>\n<div class=\"card\">\n<h3>\ud83d\udcca Clinical Data Svs Associate \u2013 Mumbai<\/h3>\n<p>\n\ud83d\udcb0 <b>Estimated Salary:<\/b> \u20b95 \u2013 \u20b98 LPA\n<\/p>\n<p><b>\ud83c\udf93 Qualification<\/b><\/p>\n<p><b>\ud83e\uddd1\u200d\ud83d\udcbb Experience Required<\/b><\/p>\n<p><b>\ud83d\udccc Key Responsibilities<\/b><\/p>\n<ul>\n<li>Manage and process clinical trial datasets<\/li>\n<li>Support clinical data validation and analysis<\/li>\n<li>Handle data integration and standardization activities<\/li>\n<li>Ensure regulatory compliance and data quality<\/li>\n<li>Collaborate with internal clinical teams<\/li>\n<li>Perform reporting and operational tasks<\/li>\n<\/ul>\n<p><b>\u2b50 Required Skills<\/b><\/p>\n<ul>\n<li>Clinical Data Management knowledge<\/li>\n<li>SAS Clinical understanding<\/li>\n<li>Analytical and problem-solving abilities<\/li>\n<li>Team collaboration skills<\/li>\n<li>Ability to work in rotational shifts<\/li>\n<\/ul>\n<\/div>\n<p><!--REGULATORY--><\/p>\n<div class=\"card\">\n<h3>\ud83d\udcc2 LifeScience Regulatory Svs Analyst \u2013 Bengaluru<\/h3>\n<p>\n\ud83d\udcb0 <b>Estimated Salary:<\/b> \u20b97 \u2013 \u20b910 LPA\n<\/p>\n<p><b>\ud83c\udf93 Qualification<\/b><\/p>\n<p><b>\ud83e\uddd1\u200d\ud83d\udcbb Experience Required<\/b><\/p>\n<p><b>\ud83d\udccc Key Responsibilities<\/b><\/p>\n<ul>\n<li>Support global regulatory submissions and filings<\/li>\n<li>Handle CMC submissions and annual reports<\/li>\n<li>Process electronic regulatory submissions<\/li>\n<li>Coordinate regulatory documentation activities<\/li>\n<li>Ensure compliance with global regulatory standards<\/li>\n<li>Manage lifecycle submission activities<\/li>\n<\/ul>\n<p><b>\u2b50 Required Skills<\/b><\/p>\n<ul>\n<li>Regulatory Affairs experience<\/li>\n<li>Stakeholder management<\/li>\n<li>Client communication abilities<\/li>\n<li>Strong documentation handling<\/li>\n<li>Adaptability and deadline management<\/li>\n<\/ul>\n<\/div>\n<p><!--PV--><\/p>\n<div class=\"card\">\n<h3>\ud83d\udc8a Pharmacovigilance Services Analyst \u2013 Bengaluru<\/h3>\n<p>\n\ud83d\udcb0 <b>Estimated Salary:<\/b> \u20b98 \u2013 \u20b912 LPA\n<\/p>\n<p><b>\ud83c\udf93 Qualification<\/b><\/p>\n<p><b>\ud83e\uddd1\u200d\ud83d\udcbb Experience Required<\/b><\/p>\n<p><b>\ud83d\udccc Key Responsibilities<\/b><\/p>\n<ul>\n<li>Prepare adverse event case narratives<\/li>\n<li>Develop safety reports for clinical studies<\/li>\n<li>Author and review Risk Management Plans (RMPs)<\/li>\n<li>Perform peer quality reviews<\/li>\n<li>Support pharmacovigilance documentation activities<\/li>\n<li>Ensure compliance with SOPs and PV regulations<\/li>\n<\/ul>\n<p><b>\u2b50 Required Skills<\/b><\/p>\n<ul>\n<li>Pharmacovigilance operations expertise<\/li>\n<li>Safety writing experience<\/li>\n<li>Risk Management Plan preparation<\/li>\n<li>Clinical safety documentation knowledge<\/li>\n<li>Strong attention to detail<\/li>\n<\/ul>\n<\/div>\n<p><!--BENEFITS--><\/p>\n<div class=\"card\">\n<h3>\ud83c\udf0d Benefits of Working at Accenture<\/h3>\n<ul>\n<li>Global work environment<\/li>\n<li>Career growth opportunities<\/li>\n<li>Learning and development programs<\/li>\n<li>Exposure to global pharmaceutical clients<\/li>\n<li>Technology-driven healthcare projects<\/li>\n<li>Inclusive workplace culture<\/li>\n<li>Cross-functional industry experience<\/li>\n<\/ul>\n<\/div>\n<p><!--RESUME--><\/p>\n<div class=\"card\">\n<h3>\ud83d\udcc4 Resume &amp; Interview Tips<\/h3>\n<ul>\n<li>Highlight SAS, Regulatory, or Pharmacovigilance experience<\/li>\n<li>Mention compliance, reporting, and documentation skills<\/li>\n<li>Showcase stakeholder communication abilities<\/li>\n<li>Keep resume ATS-friendly and concise<\/li>\n<li>Add project and operational experience clearly<\/li>\n<\/ul>\n<\/div>\n<p><!--APPLY--><\/p>\n<div class=\"card\">\n<h3 style=\"text-align: center;\">\ud83d\ude80 Job Application Links<\/h3>\n<p><!-- Accenture ke saare roles ke direct explicit HTML links bina kisi delay ke --><\/p>\n<p><!-- New Helpful Professional Note Without Timer Text --><\/p>\n<div class=\"apply-note\" style=\"margin-top: 20px;\">\n<p>\ud83d\udccc <b>Important Note Before You Apply:<\/b><\/p>\n<p>Please make sure to read the complete job description carefully before submitting your application. 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