Regulatory Affairs Associate
US$125,500 – US$177,500 / yr base salary
Posted 23 Sep 2026
Advertised as “Senior Associate, Regulatory Affairs”
BranchFactor Summary
The original posting with the fluff stripped out
- Expected experience
- 3+ yrs
- Management level
- Individual contributor
- Visa sponsorship
- Not offered
| Base salary | US$125,500 – US$177,500 / yr |
|---|
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 Senior Associate, Regulatory Operations will report to the Director of Regulatory Operations and will support various regulatory activities. The Senior Associate will work with members of the Regulatory group, other departments, and vendors to manage regulatory requirements and submissions.
Responsibilities:
- Compile, format, and publish electronic regulatory submissions to health authorities
- Supporting Regulatory Operations members with maintaining the Veeva Vault RIM system and ensuring that all regulatory records are up to date
- Supporting GxP change control processes in Veeva Vault
- Supporting the QC of regulatory documents prior to submission to health authorities
- Collaborate with external publishing vendors for e-submission files and submission receipts
- Managing the tracker with all weekly/monthly regulatory submissions and communicating information with the Regulatory group
- Maintaining templates and style guides for regulatory submissions
- Participating in the development of Standard Operating Procedures (SOPs)
- Supporting Regulatory team members with regulatory filings and projects, as needed
Preferred Skills, Qualifications and Technical Proficiencies:
- Experience with Veeva Vault systems is preferred
- Experience with electronic submissions to the EU health authority is a plus
- Detail oriented with excellent oral and written communication skills
- Strong team player, self-motivated and able to function independently as well as part of a team
- Able to work on multiple projects concurrently and adapt to a continuously changing environment