[Skip to main content](#main-content) [OpenNash Jobs](https://jobs.opennash.com/) [Hiring report](/reports/hiring/) · [All IQVIA jobs](https://jobs.opennash.com/companies/iqvia/) · [Search jobs](/search/) IQVIA · Dubai, United Arab Emirates # Global Regulatory Affairs Manager (homebased) Dubai, United Arab Emirates Manager or lead Legal & Compliance Listed on IQVIA’s official careers site. Listed as of October 17, 2026. Check that it is still open and apply there. [Apply on IQVIA’s careers site →](https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Dubai-United-Arab-Emirates/Regulatory-Affairs-Manager_R1270299) [OpenNash Jobs](https://jobs.opennash.com/) / [IQVIA](https://jobs.opennash.com/companies/iqvia/) / Global Regulatory Affairs Manager (homebased) ## Job description No visa or accommodation sponsorship You will be responsible for regulatory activities required at a country level for pharmaceutical products, including maintenance and approvals, marketing authorization transfers, communication with the Health Authority, artwork approval etc. ensuring regulatory compliance in the applicable market(s) As part of the IQVIA Global Regulatory Affairs department, you will be working with our clients – global pharmaceutical companies. ### Essential Functions - Manage the local regulatory submission preparation in collaboration with internal and external stakeholders based on the agreed strategy for designated countries - Submit submissions such as renewals/ variations/ new applications filings/ MAH transfers to the local Health Authority and EMA and follow up on the local regulatory approval process for designated countries - Preparation of local Product Labelling (e.g. SmPC, PIL), in local language for designated countries - Artwork review and approval in client systems - Manage multiple pharmaceutical products - Act as subject matter expert in regulatory processes - Acts as a Regulatory Team Leader on more complex projects, which may include authoring of regulatory documentation, filling application forms. - Establishes relationships with customers; may meet face to face to discuss regulatory issues, present lessons learned and discuss customer comments - Acts as a Subject matter expert in Regulatory knowledge in Chemistry, Manufacturing and Controls or Lifecycle Maintenance / Marketing Authorization Transfers / Labeling/ Publishing. - Project budget management - Give guidance to junior colleagues, including feedback on the quality of technical documents, and may assist in their training and development - possible exposure to present to clients on complex regulatory processes bid defense meetings - Act as reviewer for regulatory standard operating procedures - Prepare and deliver internal regulatory training if required ### MINIMUM REQUIRED EDUCATION AND EXPERIENCE Experience Typically requires 8-10+ years of prior relevant experience. ### Education Master's Degree in Life science or related discipline ### Skills and Abilities Good understanding of the Research and Development process (Chemistry, Manufacturing & Controls) relevant regulatory guideline related guidelines Possesses a specific regulatory or technical expertise Interpersonal communication (oral and written) and organization skills - Ability to establish and maintain effective working relationships with coworkers, managers and clients - Demonstrates self-motivation and enthusiasm - Ability to adapt quickly to a rapidly changing environment - Knowledge of Maintenance of marking Authorization Experience of preparing variation, renewal packages and artwork approvals. Fluent in English language and able to effectively communicate complex business language to those who speak English as a second language. Must be fluent in Arabic #LI-Remote IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at [https://jobs.iqvia.com](https://jobs.iqvia.com) ## At a glance - Posted by the employer: Not stated - First seen by OpenNash: Jul 10, 2026 - Last checked: Oct 17, 2026 - Listed for: 99 days - Location: Dubai, United Arab Emirates[Apply on IQVIA’s careers site →](https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Dubai-United-Arab-Emirates/Regulatory-Affairs-Manager_R1270299) ## More jobs at IQVIA ### [Experienced Clinical Research Associate - Multi Sponsored](https://jobs.opennash.com/companies/iqvia/jobs/9a3ffd85dea0db1fc059/) Dubai, United Arab Emirates ### [Assoc Dir, Legal](https://jobs.opennash.com/companies/iqvia/jobs/612e5463a61af7431863/) Shanghai, China ### [Associate Program Director, Regulatory Affairs](https://jobs.opennash.com/companies/iqvia/jobs/0f0aa837982610c3d139/) ### [Associate Program Director, Regulatory Affairs](https://jobs.opennash.com/companies/iqvia/jobs/961dae3c2f6cf12a5cc5/) Bucuresti, Romania ### [Associate Program Director, Regulatory Affairs](https://jobs.opennash.com/companies/iqvia/jobs/a1bfef9c01afbbc70093/) Warsaw, Poland ## Similar jobs at other companies ### [Senior Regulatory Specialist I - Toxicology, Global Regulatory Affairs](https://jobs.opennash.com/companies/ecolab/jobs/a7f265c77c592a38c347/) Ecolab · Pune, Mahārāshtra, India ### [Principal Regulatory Affairs Specialist (Global Clinical Trial Applications)](https://jobs.opennash.com/companies/thermo-fisher-scientific/jobs/75dd5c37a684a8e82c40/) Thermo Fisher Scientific · Remote, Serbia ### [Global Regulatory & Public Affairs Specialist, Motion IEC Low voltage Motors](https://jobs.opennash.com/companies/abb/jobs/239efc1c6771bdca6e40/) ABB · Vaesteras, Vastmanland County, Sweden ### [Head of Global Regulatory Strategy, Global Regulatory Affairs](https://jobs.opennash.com/companies/viatris/jobs/adaae65178e1018a1be3/) Viatris · Northern Cross, Dublin, Ireland ### [Regulatory Affairs Specialist](https://jobs.opennash.com/companies/ecolab/jobs/2f207cd244cb549328ab/) Ecolab · Kraków, Poland OpenNash lists jobs from employers’ own careers sites and does not handle applications. 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