New · posted Oct 15
Corcept Therapeutics · Pharmaceuticals
Senior Associate, Regulatory Affairs
- Redwood City, CA
- On-site
- Full-time
- Senior & Principal
Open until filled
The role
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.
What you need
Preferred Education and Experiencenice to have
- BA/BS degree in a scientific discipline
- 3+ years of relevant regulatory experience in the pharmaceutical industry
Applicants must be currently authorized to work in the United States on a full-time basis.
Corcept appreciates the commitment and hard work of all our team members as we strive to discover and develop novel treatments for patients with serious unmet medical needs.
Preferred Skills, Qualifications and Technical Proficienciesnice to have
- 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
- Proficient in organization, prioritization, and time management
- Experience with Microsoft Word, PowerPoint and Excel
What you'll do
- 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
Pay
$125,600 – $177,300 a year
Employer providedThe pay range that the Company reasonably expects to pay for this headquarters-based position is $125,600-$177,300; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.
Where you'll work
Redwood City, CAOn-siteOpen in Maps (opens in a new tab)
More jobs in Redwood City, CAEqual opportunity, accessibility and legal noticesCorcept Therapeutics's statements, word for word
Corcept is an Equal Opportunity Employer
Corcept will not conduct interviews via text message or messaging platforms and will not ask you to download anything as part of your interview. Though we use third-party tools to help with advertising our jobs, please be vigilant in checking that the communication is in fact coming from Corcept.
For information on how Corcept collects, uses, discloses, protects, and otherwise processes personal information and an explanation of the rights and choices available to you with respect to your personal information, please refer to our Privacy Notice link.
Job intelligence
The context around this role
Live data · October 15, 2026
Salary intelligence
How the pay compares
This roleEmployer provided
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $125,600 | — | $177,300 |
This role: Corcept Therapeutics's own published range.
Career trajectory
Where this role sits in Regulatory Operations
The general path across 34 open Regulatory Operations roles on Regulatory Jobs, with the titles they carry most. Not Corcept Therapeutics's own promotion track.
Career resources on Regulatory Operations
Skills DNA
What this role leans on
How many of the posting's 24 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Regulatory submissions7
- Collaboration and leadership6
- Documentation and SOPs4
- Data and digital systems4
- GMP and compliance1
- Quality systems and risk1
Company hiring pulse
Corcept Therapeutics on Regulatory Jobs
- 5
- Open roles
- 5
- Distinct roles
- 1
- Locations
By discipline
- Quality2 40%
- Compliance & Safety2 40%
- Regulatory1 20%
By level
- Manager3 60%
- Director1 20%
- Senior & Principal1 20%
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Senior Associate, Regulatory Affairs at Corcept Therapeutics
Open until filled. $126K–$177K a year, employer provided.