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⏰ Full-time

Clinical Content and Regulatory Affairs Manager

vueverse.
Location 📍 Bengaluru, India
Posted 📅 June 01, 2026
Work Type ⏰ Full-time

Position Overview

Role Overview

You will lead end-to-end medical writing and content submission operations, ensuring all deliverables are scientifically accurate, compliant with brand and AMA guidelines, and delivered on time. The role combines scientific leadership, people management, and operational oversight, including MLR readiness and quality governance.


Key Responsibilities

Content & Scientific Leadership

  • Oversee development and review of scientific and medical content (manuscripts, abstracts, slide decks, posters, digital assets)
  • Interpret clinical data and translate it into clear, audience-appropriate communication
  • Ensure adherence to AMA style, brand guidelines, and regulatory standards
  • Conduct rigorous QC, proofreading, and fact-checking


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Job Details

Employment Type
Full-time
📊
Category
Other Management Occupations
🏠
Work Arrangement
On-site
📍
Location
Bengaluru, India