{"id":6131,"date":"2026-07-08T13:53:56","date_gmt":"2026-07-08T13:53:56","guid":{"rendered":"https:\/\/globalpharmajobs.org\/?job_listing=safety-data-management-job-at-pfizer"},"modified":"2026-07-08T13:53:56","modified_gmt":"2026-07-08T13:53:56","slug":"safety-data-management-job-at-pfizer","status":"publish","type":"job_listing","link":"https:\/\/globalpharmajobs.org\/?job_listing=safety-data-management-job-at-pfizer","title":{"rendered":"Safety Data Management Job at Pfizer"},"content":{"rendered":"<p><br \/>\n<\/p>\n<div>\n<p class=\"wp-block-paragraph\">Pfizer is a leading global biopharmaceutical company committed to discovering, developing, and providing innovative healthcare solutions. Our\u00a0<strong>Worldwide Medical and Safety<\/strong>\u00a0team plays a crucial role in ensuring evidence-based medical decisions, improving patient health outcomes, and maintaining the highest safety standards for medicines worldwide.<\/p>\n<p class=\"wp-block-paragraph\">At Pfizer, we believe in\u00a0<strong>using your power for purpose<\/strong>\u2014whether it\u2019s ensuring scientific accuracy, addressing data gaps, or collaborating with healthcare stakeholders to promote the safe use of medicines.<\/p>\n<h2 class=\"wp-block-heading\"><strong>Job Description: Associate \u2013 Safety Data Management Specialist<\/strong><\/h2>\n<h3 class=\"wp-block-heading\"><strong>Primary Responsibilities<\/strong><\/h3>\n<p class=\"wp-block-paragraph\">As an\u00a0<strong>Associate \u2013 Safety Data Management Specialist<\/strong>, you will be responsible for:<\/p>\n<ul class=\"wp-block-list\">\n<li><strong>Case Processing Activities:<\/strong>\n<ul class=\"wp-block-list\">\n<li>Reviewing, ranking, verifying, and documenting case-related information (event terms, validity, seriousness, timelines).<\/li>\n<li>Ensuring accuracy and consistency in case processing.<\/li>\n<li>Writing and editing case narratives.<\/li>\n<li>Determining and executing appropriate case follow-ups, including generating follow-up requests.<\/li>\n<\/ul>\n<\/li>\n<li><strong>Compliance &amp; Quality Checks:<\/strong>\n<ul class=\"wp-block-list\">\n<li>Reviewing processed cases for accuracy, consistency, and compliance with regulatory standards.<\/li>\n<li>Identifying complex cases and escalating them as needed.<\/li>\n<\/ul>\n<\/li>\n<li><strong>Regulatory &amp; Safety Expertise:<\/strong>\n<ul class=\"wp-block-list\">\n<li>Staying updated on\u00a0<strong>global safety regulations<\/strong>,\u00a0<strong>SOPs<\/strong>, and\u00a0<strong>data entry conventions<\/strong>.<\/li>\n<li>Determining reportability of scheduled reports in line with regulatory requirements.<\/li>\n<\/ul>\n<\/li>\n<li><strong>Collaboration:<\/strong>\n<ul class=\"wp-block-list\">\n<li>Liaising with internal and external stakeholders for\u00a0<strong>safety data collection and reconciliation<\/strong>.<\/li>\n<li>Participating in safety-related activities as required.<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<h3 class=\"wp-block-heading\"><strong>Eligibility Criteria (Minimum Requirements)<\/strong><\/h3>\n<ul class=\"wp-block-list\">\n<li><strong>Education:<\/strong>\u00a0<strong>B.Pharm, M.Pharm, or Pharm.D only<\/strong>.<\/li>\n<li><strong>Experience:<\/strong>\u00a0<strong>1-2 years<\/strong>\u00a0in\u00a0<strong>end-to-end ICSR (Individual Case Safety Report) processing<\/strong>, including listedness assessment.<\/li>\n<li><strong>Skills:<\/strong>\n<ul class=\"wp-block-list\">\n<li>Ability to work in a\u00a0<strong>team environment<\/strong>.<\/li>\n<li>Strong attention to detail.<\/li>\n<\/ul>\n<\/li>\n<\/ul>\n<h3 class=\"wp-block-heading\"><strong>Preferred Qualifications (Bonus Points If You Have)<\/strong><\/h3>\n<ul class=\"wp-block-list\">\n<li>Hands-on experience with\u00a0<strong>ARGUS safety database<\/strong>.<\/li>\n<li>Proficiency in processing\u00a0<strong>E2B R2 and R3 (XML format)<\/strong>\u00a0source documents.<\/li>\n<li>Good understanding of\u00a0<strong>medical terminology<\/strong>\u00a0and\u00a0<strong>global drug safety regulations<\/strong>.<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\"><strong>Work Location &amp; Assignment<\/strong><\/h2>\n<ul class=\"wp-block-list\">\n<li><strong>Hybrid work model<\/strong>\u00a0(combination of in-office and remote work).<\/li>\n<li><strong>Location:<\/strong>\u00a0<strong>Chennai, India<\/strong>.<\/li>\n<\/ul>\n<p class=\"wp-block-paragraph\"><strong>Location:<\/strong>\u00a0Chennai, India<br \/><strong>Job Type:<\/strong>\u00a0Full-time<br \/><strong>Posted:<\/strong>\u00a0Today<br \/><strong>Requisition ID:<\/strong>\u00a04939465<\/p>\n<h2 class=\"wp-block-heading\"><strong>Why Join Pfizer?<\/strong><\/h2>\n<ul class=\"wp-block-list\">\n<li><strong>Global Impact:<\/strong>\u00a0Contribute to life-saving medical advancements.<\/li>\n<li><strong>Career Growth:<\/strong>\u00a0Opportunities for professional development in pharmacovigilance and drug safety.<\/li>\n<li><strong>Inclusive Culture:<\/strong>\u00a0Pfizer is an\u00a0<strong>equal opportunity employer<\/strong>, fostering diversity and inclusion.<\/li>\n<\/ul>\n<h2 class=\"wp-block-heading\"><strong>How to Apply<\/strong><\/h2>\n<p class=\"wp-block-paragraph\">Interested candidates can apply through Pfizer\u2019s official career portal using\u00a0<strong>Requisition ID: 4939465<\/strong>.<\/p>\n<p class=\"wp-block-paragraph\"><strong><a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/pfizer.wd1.myworkdayjobs.com\/en-US\/PfizerCareers\/job\/Associate---Safety-Data-Management-Specialist_4939465\" target=\"_blank\" rel=\"noreferrer noopener nofollow\">Application Link<\/a><\/strong><\/p>\n<\/div>\n<p><br \/>\n<br \/><a href=\"https:\/\/pharmabharat.org\/safety-data-management-job-at-pfizer\/\">Source link <\/a><\/p>\n","protected":false},"author":1,"featured_media":6132,"template":"","meta":{"_promoted":"","_job_location":"","_application":"","_company_name":"","_company_website":"","_company_tagline":"","_company_twitter":"","_company_video":"","_filled":0,"_featured":0,"_remote_position":0,"_job_salary":"","_job_salary_currency":"","_job_salary_unit":""},"job_listing_region":[],"job-categories":[166],"job-types":[],"job_listing_tag":[],"class_list":["post-6131","job_listing","type-job_listing","status-publish","has-post-thumbnail","hentry","job_listing_category-cdm"],"_links":{"self":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=\/wp\/v2\/job-listings\/6131","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=\/wp\/v2\/job-listings"}],"about":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=\/wp\/v2\/types\/job_listing"}],"author":[{"embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=\/wp\/v2\/users\/1"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=\/wp\/v2\/media\/6132"}],"wp:attachment":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=6131"}],"wp:term":[{"taxonomy":"job_listing_region","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_region&post=6131"},{"taxonomy":"job_listing_category","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-categories&post=6131"},{"taxonomy":"job_listing_type","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-types&post=6131"},{"taxonomy":"job_listing_tag","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_tag&post=6131"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}