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Regulatory Affairs Officer/Associate Director

IQVIA | Singapore, Singapore | Posted June 24, 2026

Position Overview

Job Overview
Prepares and/or reviews regulatory submissions to support clinical trial and marketing authorisation activities for either internal and/or external clients. Independently provides regulatory support for more complex projects.

Essential Functions

  • Acts as a Regulatory Team Leader on complex projects, which may include technical writing and/or may act as a Project Manager for a stand-alone project, with guidance from senior staff as appropriate.

  • Competently writes regulatory and/or technical documents with minimal review by senior staff.

  • Establishes relationships with many customers; may meet face to face without rest of team to discuss regulatory issues and present lessons learned. Adopts a proactive and flexible approach to resolve any issues.

  • Undertakes detailed review and management of budgets related to projects, including out of scope activities. Ensures revenue is recognised and challenge...

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