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Regulatory Affairs Specialist

1 week ago

Bengaluru, Karnataka, India Biotech Healthcare Full time
Key Responsibilities

The Regulatory Affairs Specialist - Clinical Trials will oversee clinical trial execution from initiation to close-out, register clinical trials on various regulatory platforms as per local regulations, and ensure timely data collection from sites for ongoing projects.

  • Oversee clinical trial execution from initiation to close-out.
  • Register clinical trials on various regulatory platforms as per local regulations.
Behavioral Skills Required
  • Proactive approach with a commitment to process improvement.
  • Ability to work independently and detail-oriented with strong organizational skills.