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
$186k - $233k
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