Regulatory Associate I — Hybrid, Global Submissions

Corcept Therapeutics Incorporated; Redwood City (CA); Hybrid; USD 84,000 - 99,000; Full time

Job summary

Corcept Therapeutics Incorporated, headquartered in Redwood City, California, is seeking an Associate to support Regulatory leadership in global nonclinical and clinical regulatory strategies, preparing for health authority interactions and submissions. This hybrid role typically requires on-site presence three days per week.

Responsibilities include preparing regulatory documents, coordinating with external partners, tracking submission timelines, and maintaining up-to-date regulatory

Qualifications

• Bachelor’s degree required.
• Advanced degree (MS, PharmD, PhD) preferred.
• Minimum 1–2 years of clinical regulatory experience.

Responsibilities

• Participates in cross-functional teams supporting clinical studies to develop Corcept products.
• Assists with the preparation, review, and submission of regulatory documents.
• Supports preparation for health authority interactions and meetings, including briefing materials, responses, and follow-up documentation.
• Coordinates with CROs and external partners supporting global regulatory submissions and health authority correspondence.
• Collaborates with Regulatory Operations to provide final documents and perform quality-control reviews of submission outputs.
• Supports submission and maintenance of IND applications and clinical trial applications.

Skills

Interpersonal skills

Initiative

Adaptability

Multitasking

Team collaboration

Education

Bachelor’s degree

Advanced degree preferred (MS/PharmD/PhD)

Job description

Corcept Therapeutics Incorporated, headquartered in Redwood City, California, is seeking an Associate to support Regulatory leadership in global nonclinical and clinical regulatory strategies, preparing for health authority interactions and submissions. This hybrid role typically requires on-site presence three days per week.

Responsibilities include preparing regulatory documents, coordinating with external partners, tracking submission timelines, and maintaining up-to-date regulatory