Senior Regulatory Affairs Consultant

Parexel

Multiple Locations
11+ years of relevant experience
Knowledge of eu/us regulatory procedures
Experience in handling cmc related queries
At Parexel, we share the goal of improving the world's health through clinical development solutions. Each team member contributes to the development of therapies that benefit patients, demonstrating empathy and commitment. The role involves leading regulatory submissions and ensuring compliance with evolving guidelines across various markets

Job Summary

  • At Parexel, we share the goal of improving the world's health through clinical development solutions. Each team member contributes to the development of therapies that benefit patients, demonstrating empathy and commitment. The role involves leading regulatory submissions and ensuring compliance with evolving guidelines across various markets.

Matching Summary

At Parexel, we share the goal of improving the world's health through clinical development solutions. Each team member contributes to the development of therapies that benefit patients, demonstrating empathy and commitment. The role involves leading regulatory submissions and ensuring compliance with evolving guidelines across various markets.

Skills & Requirements

Must-have

  • 11+ years of relevant experience
  • knowledge of EU/US regulatory procedures
  • experience in handling CMC related queries

Nice-to-have

  • strong communication skills
  • ability to guide and mentor
  • familiarity with EU Guidelines

Key Requirements

  • experience in life cycle management
  • working knowledge of RIMS like Veeva Vault

Work Rights

Not specified

Tailored Resume

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