{"id":5967,"date":"2026-07-07T08:12:22","date_gmt":"2026-07-07T08:12:22","guid":{"rendered":"https:\/\/globalpharmajobs.org\/?job_listing=iqvia-hiring-for-clinical-data-management-professional"},"modified":"2026-07-07T08:12:22","modified_gmt":"2026-07-07T08:12:22","slug":"iqvia-hiring-for-clinical-data-management-professional","status":"publish","type":"job_listing","link":"https:\/\/globalpharmajobs.org\/?job_listing=iqvia-hiring-for-clinical-data-management-professional","title":{"rendered":"IQVIA Hiring For Clinical Data Management Professional"},"content":{"rendered":"<p><br \/>\n<\/p>\n<div>\n<p class=\"wp-block-paragraph\">Are you an experienced <strong>Clinical Data Management professional<\/strong> looking for your next career move in the pharmaceutical and clinical research industry? IQVIA is conducting a <strong>walk-in interview for Clinical Data Management professionals<\/strong> on <strong>27th February 2026 (Friday)<\/strong> at its Thane office.<\/p>\n<p class=\"wp-block-paragraph\">This opportunity is ideal for candidates with <strong>4+ years of Clinical Data Management experience<\/strong>, strong expertise in <strong>Veeva EDC<\/strong>, and hands-on exposure to <strong>end-to-end clinical data management processes<\/strong> across the study lifecycle.<\/p>\n<p class=\"wp-block-paragraph\">If you are seeking Clinical Data Management jobs in Thane or exploring CRO career opportunities in India, this hiring drive could be your next big step.<\/p>\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n<h2 class=\"wp-block-heading\">\ud83d\udcc5 Walk-In Interview Details<\/h2>\n<ul class=\"wp-block-list\">\n<li><strong>Position:<\/strong> Clinical Data Management Professional<\/li>\n<li><strong>Experience Required:<\/strong> Minimum 4 years<\/li>\n<li><strong>Interview Date:<\/strong> 27th February 2026 (Friday)<\/li>\n<li><strong>Location:<\/strong> Thane, Maharashtra<\/li>\n<li><strong>Mode:<\/strong> Walk-In Interview<\/li>\n<\/ul>\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n<h2 class=\"wp-block-heading\">\ud83d\udd0d Key Responsibilities \u2013 Clinical Data Management<\/h2>\n<p class=\"wp-block-paragraph\">Selected candidates for the Clinical Data Management role will be responsible for:<\/p>\n<ul class=\"wp-block-list\">\n<li>Managing <strong>end-to-end Clinical Data Management processes<\/strong><\/li>\n<li>Supporting <strong>clinical trial start-up, conduct, and close-out activities<\/strong><\/li>\n<li>Designing and reviewing <strong>eCRFs (electronic Case Report Forms)<\/strong><\/li>\n<li>Performing <strong>data validation, discrepancy management, and query resolution<\/strong><\/li>\n<li>Ensuring compliance with <strong>ICH-GCP guidelines and regulatory standards<\/strong><\/li>\n<li>Coordinating with cross-functional teams including Clinical Operations, Biostatistics, and Medical Writing<\/li>\n<li>Maintaining data integrity in <strong>Veeva and Veeva EDC platforms<\/strong><\/li>\n<li>Contributing to database lock and study close-out deliverables<\/li>\n<\/ul>\n<p class=\"wp-block-paragraph\">This Clinical Data Management job requires strong analytical skills and deep familiarity with clinical trial data workflows.<\/p>\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n<h2 class=\"wp-block-heading\">\u2705 Qualifications &amp; Skills Required<\/h2>\n<p class=\"wp-block-paragraph\">To qualify for this Clinical Data Management opportunity, candidates should have:<\/p>\n<ul class=\"wp-block-list\">\n<li>Minimum <strong>4 years of relevant industry experience in Clinical Data Management<\/strong><\/li>\n<li>Experience across the <strong>full clinical study lifecycle<\/strong><\/li>\n<li>Hands-on expertise in <strong>Veeva and Veeva EDC<\/strong><\/li>\n<li>Strong understanding of <strong>CDISC standards, GCP, and regulatory requirements<\/strong><\/li>\n<li>Experience working in a <strong>CRO or pharmaceutical company<\/strong><\/li>\n<li>Excellent documentation and communication skills<\/li>\n<\/ul>\n<p class=\"wp-block-paragraph\">Professionals with prior exposure to global clinical trials and regulatory submissions will have an added advantage.<\/p>\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n<h2 class=\"wp-block-heading\">\ud83d\udcbc Why Consider This Clinical Data Management Role?<\/h2>\n<p class=\"wp-block-paragraph\">Working in Clinical Data Management at a leading CRO offers:<\/p>\n<ul class=\"wp-block-list\">\n<li>Exposure to <strong>global clinical trials<\/strong><\/li>\n<li>Opportunity to work with advanced <strong>Veeva EDC platforms<\/strong><\/li>\n<li>Career growth in the <strong>clinical research and pharmaceutical industry<\/strong><\/li>\n<li>Competitive salary structure<\/li>\n<li>Professional development and training programs<\/li>\n<li>Collaborative and innovation-driven work culture<\/li>\n<\/ul>\n<p class=\"wp-block-paragraph\">This role is particularly suitable for professionals seeking <strong>Clinical Data Management jobs in Maharashtra<\/strong> or advancement in CRO data management careers.<\/p>\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n<h2 class=\"wp-block-heading\">\ud83d\udcb0 Salary Range (Indicative)<\/h2>\n<ul class=\"wp-block-list\">\n<li><strong>\u20b98,00,000 \u2013 \u20b914,00,000 per annum (INR)<\/strong><\/li>\n<li>Based on experience, expertise in Veeva EDC, and clinical trial exposure<\/li>\n<\/ul>\n<hr class=\"wp-block-separator has-alpha-channel-opacity\"\/>\n<h2 class=\"wp-block-heading\">\ud83d\udce7 How to Apply<\/h2>\n<p class=\"wp-block-paragraph\">Interested candidates with relevant Clinical Data Management experience can share their updated CV at:<\/p>\n<p class=\"wp-block-paragraph\">\ud83d\udce9 <strong><a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/pharmabharat.org\/iqvia-hiring-for-clinical-data-management-professional\/mailto:jinto.jacobc@iqvia.com\" target=\"_blank\" rel=\"noreferrer noopener nofollow\">jinto.jacobc@iqvia.com<\/a><\/strong><\/p>\n<\/div>\n<p><br \/>\n<br \/><a href=\"https:\/\/pharmabharat.org\/iqvia-hiring-for-clinical-data-management-professional\/\">Source link <\/a><\/p>\n","protected":false},"author":1,"featured_media":5968,"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-5967","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\/5967","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\/5968"}],"wp:attachment":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=5967"}],"wp:term":[{"taxonomy":"job_listing_region","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_region&post=5967"},{"taxonomy":"job_listing_category","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-categories&post=5967"},{"taxonomy":"job_listing_type","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-types&post=5967"},{"taxonomy":"job_listing_tag","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_tag&post=5967"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}