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Associate I, Regulatory Affairs

Corcept Therapeutics

Corcept Therapeutics seeks a regulatory affairs associate to support clinical and nonclinical regulatory strategy development, health authority interactions, and global submissions for cortisol-modulating therapeutics. The hybrid role involves cross-functional collaboration to advance products through regulatory pathways.

Responsibilities

  • Support preparation, review, and submission of regulatory documents and submissions
  • Coordinate with clinical research organizations and health authorities on global submissions
  • Assist in organizing briefing materials and responses for health authority meetings
  • Track regulatory timelines, deliverables, and health authority commitments
  • Collaborate with nonclinical and clinical teams to compile documents for regulatory filings

Requirements

  • Bachelor's degree required; advanced degree in life sciences preferred
  • Strong interpersonal and written communication abilities
  • Ability to manage multiple assignments concurrently with attention to timelines
  • Proactive problem-solving and adaptability to shifting priorities
  • Experience working collaboratively within cross-functional teams
Vacancy posted 8 days ago
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