Job Description

OVERVIEW OF ROLE – CLINICAL PROFILE

Based in our India office (Bangalore / Gurgaon), we seek a skilled Individual contributor proficient in applying subject matter expertise. The successful candidate will be responsible for the creation and upkeep of high-quality regulatory intelligence content focusing on Clinical Trial Data. Responsibilities also include managing day-to-day operations for IQVIA Regulatory Intelligence, covering planning, client delivery, and maintaining quality standards.

RESPONSIBILITIES

  • Prepares, reviews, and updates regulatory documentation in the area of clinical trials based on documents published by regulatory authorities as appropriate with particular focus on APAC region and EU region.
  • Works within cross-functional teams and collaborates with a network of internal/external regulatory experts to ensure the production and maintenance of high-quality (timeliness, completeness, and accuracy) regulatory intelligence rel...

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