Principal Clinical Trial Regulatory Affairs (ctra)

SyneosHealth

Clinical trial regulatory affairs expertise
Drug development lifecycle knowledge
Fda and ema regulatory compliance
The role involves partnering with innovators to navigate complexity and accelerate drug development progress

Job Summary

  • The role involves partnering with innovators to navigate complexity and accelerate drug development progress.
  • Syneos Health has worked with 94% of all Novel FDA Approved Drugs in the past 5 years.
  • The company is committed to building an inclusive culture where colleagues can authentically be themselves.

Matching Summary

The role involves partnering with innovators to navigate complexity and accelerate drug development progress.

Skills & Requirements

Must-have

  • Clinical trial regulatory affairs expertise
  • Drug development lifecycle knowledge
  • FDA and EMA regulatory compliance

Nice-to-have

  • Passion for patient progress
  • Agile problem-solving mindset
  • Collaborative team environment

Key Requirements

  • Years of experience in clinical trial regulatory affairs
  • Deep expertise in drug development
  • Ability to represent customer needs in solutions

Work Rights

Not specified

Tailored Resume

Cover Letter