Regulatory Affairs Associate
US$84,500 – US$99,500 / yr base salary
Posted 15 Oct 2026
Advertised as “Associate I, Regulatory Affairs”
BranchFactor Summary
The original posting with the fluff stripped out
- Level
- I
- Expected experience
- 1–2 yrs
- Management level
- Individual contributor
- Employment
- Hybrid
- Visa sponsorship
- Not offered
| Base salary | US$84,500 – US$99,500 / yr |
|---|
Study levelBachelor's
Field of studyChemistry, Life Sciences, Molecular Biology (or related)
Study levelMaster's or higher
For more than 25 years, Corcept has been singularly focused on the science of cortisol, a powerful hormone that when unregulated, can play a role in a broad range of diseases.
Our commercial portfolio includes treatments for hypercortisolism and oncology, and the company has discovered more than 1,000 proprietary selective cortisol modulators and glucocorticoid receptor antagonists. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today.
Corcept is headquartered in Redwood City, California. To learn more, visit www.corcept.com.
The Associate supports Regulatory leadership in development and execution of global nonclinical and clinical regulatory strategies, preparing for health authority interactions and supporting regulatory submissions. The Associate works with internal cross functional study team members and external parties (e.g., health authorities, vendors, and consultants) to maintain up-to-date information on regulatory requirements and submissions.
This is a hybrid role that typically requires on-site presence three days per week.
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 clinical research organizations and other external partners supporting global regulatory submissions and health authority correspondence
- Collaborates with nonclinical, clinical, and other cross-functional teams to collect and compile documents for global regulatory submissions
- Collaborates with Regulatory Operations to provide final documents and performs quality-control reviews of published submission outputs
- Supports the submission and maintenance of investigational new drug applications and clinical trial applications
- Supports the maintenance of marketed product applications (i.e., NDAs and MAAs)
- Supports regulatory reporting requirements for investigational and marketed products