{"id":9052,"date":"2026-10-08T20:37:38","date_gmt":"2026-10-08T20:37:38","guid":{"rendered":"https:\/\/globalpharmajobs.org\/?job_listing=cliantha-research-clinical-data-analyst-walk-in"},"modified":"2026-10-08T20:37:38","modified_gmt":"2026-10-08T20:37:38","slug":"cliantha-research-clinical-data-analyst-walk-in","status":"publish","type":"job_listing","link":"https:\/\/globalpharmajobs.org\/?job_listing=cliantha-research-clinical-data-analyst-walk-in","title":{"rendered":"Cliantha Research Clinical Data Analyst Walk-In"},"content":{"rendered":"<p><br \/>\n<\/p>\n<div>\n<h2>Cliantha Research Clinical Data Analyst Walk-In \u2013 Ahmedabad<\/h2>\n<p>Cliantha Research is conducting a <strong>walk-in interview for Clinical Data Analyst<\/strong> in Ahmedabad. The opportunity is open to candidates with <strong>1\u20136 years of experience<\/strong>, with <strong>5 openings<\/strong> available. The role involves clinical data management activities including <strong>Data Management Plans, database design, CRF development, EDC, UAT, data validation, discrepancy management, medical coding, SAE reconciliation, and external data reconciliation<\/strong>. Candidates with <strong>B.Pharm, M.Sc., or M.Pharm<\/strong> qualifications can apply.<\/p>\n<h2>Clinical Data Analyst \u2013 Clinical Data Management<\/h2>\n<h3>Job Role &amp; Responsibilities<\/h3>\n<p>The Clinical Data Analyst will coordinate with the <strong>Study Lead of the Clinical Data Management (CDM) department<\/strong> to support effective study progress and departmental activities at Cliantha Research.<\/p>\n<p>Key responsibilities include:<\/p>\n<ul>\n<li>Create, maintain, and update study-specific documents such as:\n<ul>\n<li>Data Management Plan (DMP)<\/li>\n<li>Data Validation Plan<\/li>\n<li>Database Design Specifications<\/li>\n<li>External Data Handling Plan<\/li>\n<li>Other study-specific documents<\/li>\n<\/ul>\n<\/li>\n<li>Design <strong>Case Report Forms (CRFs)<\/strong> for paper-based and EDC studies and review CRF designs.<\/li>\n<li>Receive and track subject CRFs for paper-based studies.<\/li>\n<li>Coordinate with study team members for clinical data management activities.<\/li>\n<li>Perform <strong>User Acceptance Testing (UAT)<\/strong> in study databases based on established edit checks.<\/li>\n<li>Check consistency between data entry screens and Case Report Forms.<\/li>\n<li>Train clinical sites on the use of study-specific databases for <strong>Electronic Data Capture (EDC)<\/strong> studies.<\/li>\n<li>Process role-specific database access requests.<\/li>\n<li>Identify and resolve clinical data discrepancies through computerized and manual data checks.<\/li>\n<li>Perform <strong>data management quality control<\/strong> for assigned studies.<\/li>\n<li>Generate queries and update and verify DCFs and Ex-DCFs for paper-based CRF studies.<\/li>\n<li>Handle external data and perform applicable <strong>external data reconciliation<\/strong>.<\/li>\n<li>Resolve queries related to external data.<\/li>\n<li>Perform <strong>Serious Adverse Event (SAE) reconciliation<\/strong> and resolve related queries.<\/li>\n<li>Perform <strong>medical coding<\/strong> of terms reported on Case Report Forms.<\/li>\n<li>Follow Standard Operating Procedures, work procedures, and project scope requirements.<\/li>\n<li>Maintain appropriate training documentation.<\/li>\n<li>Work with external teams, programmers, statisticians, monitors, CRAs, and other project team members.<\/li>\n<li>Follow the training schedule and maintain awareness of applicable Data Management SOPs.<\/li>\n<li>Ensure appropriate archival of project data and documents according to the applicable Archival SOP.<\/li>\n<\/ul>\n<h2>Clinical Data Management Skills<\/h2>\n<p>The role provides exposure to important areas of <strong>clinical data management and clinical research<\/strong>, including:<\/p>\n<ul>\n<li>Clinical Data Management<\/li>\n<li>Clinical Data<\/li>\n<li>Data Management Plans<\/li>\n<li>Database Design<\/li>\n<li>Data Validation<\/li>\n<li>Case Report Forms<\/li>\n<li>Electronic Data Capture<\/li>\n<li>User Acceptance Testing<\/li>\n<li>Data Quality Control<\/li>\n<li>External Data Reconciliation<\/li>\n<li>SAE Reconciliation<\/li>\n<li>Medical Coding<\/li>\n<li>Clinical Trial Documentation<\/li>\n<li>SOP Compliance<\/li>\n<li>Clinical Data Archiving<\/li>\n<\/ul>\n<h2>Eligibility &amp; Qualifications<\/h2>\n<p>Candidates with <strong>1\u20136 years of experience<\/strong> in clinical data management or related clinical research activities can apply. The role is suitable for professionals with experience in clinical databases, EDC studies, data validation, discrepancy management, medical coding, and clinical trial data processes.<\/p>\n<p><strong>B.Pharm, M.Pharm, B.Sc. Science, M.Sc. Science or related qualifications.<\/strong><\/p>\n<h2>Walk-In Interview Details<\/h2>\n<p><strong>Company:<\/strong> Cliantha Research<br \/><strong>Position:<\/strong> Clinical Data Analyst<br \/><strong>Openings:<\/strong> 5<br \/><strong>Experience:<\/strong> 1\u20136 Years<br \/><strong>Salary:<\/strong> \u20b93.5\u20138.5 LPA<br \/><strong>Date:<\/strong> 10 October 2026<br \/><strong>Time:<\/strong> 9:30 AM \u2013 2:00 PM<br \/><strong>Location:<\/strong> Cliantha Research La Costa, TP 86, FP 21 &amp; 47, Off S.P. Ring Road, Near Lakshya International School, Sarkhej, Ahmedabad \u2013 382210, Gujarat, India<\/p>\n<p><strong>Contact:<\/strong> Mukund Junnarkar<\/p>\n<blockquote>\n<p><strong>Note:<\/strong> The recruitment listing mentions <strong>9:30 AM\u20132:00 PM<\/strong> in the walk-in details and <strong>9:30 AM\u20133:00 PM<\/strong> within the job description. Candidates should confirm the reporting\/closing time with the recruitment team before attending.<\/p>\n<\/blockquote>\n<p>\u00a0<\/p>\n<h2>How to Apply<\/h2>\n<p>Interested candidates can attend the <strong>Cliantha Research Clinical Data Analyst Walk-In Interview<\/strong> at the above-mentioned venue with the required documents.<\/p>\n<p>Candidates should verify the latest walk-in details before travelling.<\/p>\n<p><a rel=\"nofollow\" target=\"_blank\" href=\"https:\/\/www.naukri.com\/job-listings-clinical-data-analyst-cliantha-research-ahmedabad-1-to-6-years-081026038662\" rel=\"nofollow noopener\" target=\"_blank\">Apply \/ View Cliantha Research Clinical Data Analyst Job<\/a><\/p>\n<h2>Job Summary<\/h2>\n<div>\n<div>\n<div>\n<table>\n<thead>\n<tr>\n<th>Category<\/th>\n<th>Details<\/th>\n<\/tr>\n<\/thead>\n<tbody>\n<tr>\n<td><strong>Company<\/strong><\/td>\n<td>Cliantha Research<\/td>\n<\/tr>\n<tr>\n<td><strong>Vacancies<\/strong><\/td>\n<td>Clinical Data Analyst, 5 Openings<\/td>\n<\/tr>\n<tr>\n<td><strong>Required Education<\/strong><\/td>\n<td>B.Pharm, M.Pharm, B.Sc. Science, M.Sc. Science or related qualifications<\/td>\n<\/tr>\n<tr>\n<td><strong>Experience<\/strong><\/td>\n<td>1\u20136 Years<\/td>\n<\/tr>\n<\/tbody>\n<\/table>\n<p>https:\/\/www.naukri.com\/job-listings-clinical-data-analyst-cliantha-research-ahmedabad-1-to-6-years-081026038662?utm_source=chatgpt.com<\/p>\n<\/div>\n<\/div>\n<\/div>\n<p><!-- CONTENT END 1 -->\n\t\t\t<\/div>\n<p><br \/>\n<br \/><a href=\"https:\/\/pharmastuff.org\/job\/cliantha-research-clinical-data-analyst\">Source link <\/a><\/p>\n","protected":false},"author":1,"featured_media":9053,"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":[167],"job-types":[],"job_listing_tag":[],"class_list":["post-9052","job_listing","type-job_listing","status-publish","has-post-thumbnail","hentry","job_listing_category-medical-coding"],"_links":{"self":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=\/wp\/v2\/job-listings\/9052","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\/9053"}],"wp:attachment":[{"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=9052"}],"wp:term":[{"taxonomy":"job_listing_region","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_region&post=9052"},{"taxonomy":"job_listing_category","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-categories&post=9052"},{"taxonomy":"job_listing_type","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob-types&post=9052"},{"taxonomy":"job_listing_tag","embeddable":true,"href":"https:\/\/globalpharmajobs.org\/index.php?rest_route=%2Fwp%2Fv2%2Fjob_listing_tag&post=9052"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}