Senior Regulatory Start-Up Specialist, Global Trials

A global clinical contract research organization is seeking a Senior Regulatory Affairs Study Start Up Specialist to manage regulatory documentation for clinical studies. The role requires at least 5 years of relevant experience in pharmaceutical or CRO regulatory processes and offers an office-based position in Covington, Kentucky or Raleigh, North Carolina. As part of the team, you will advise on regulatory requirements, conduct compliance assessments, and interact with various stakeholders to ensure timely deliverables.

This role supports career progression and values work-life balance.
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