New · posted Oct 16
Corcept Therapeutics · Pharmaceuticals
Associate I, Regulatory Affairs
- Redwood City, CA
- Hybrid
- Full-time
- Associate & Specialist
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 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.
What you need
Preferred Education and Experiencenice to have
- Bachelor’s degree required. Advanced degree (M.S., Pharm.D., Ph.D.) in life sciences (including chemistry, molecular biology, or similar) preferred
- Minimum of 1-2 years of clinical regulatory experience
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
- Strong interpersonal and communication skills
- Demonstrates initiative and proactively supports project and team needs
- Adapts to changing priorities and contributes to practical, solution-oriented problem-solving
- Ability to organize and manage multiple assignments from different stakeholders while meeting established timelines and quality expectations
- Ability to work effectively both as a collaborative team member and as an individual contributor, with appropriate guidance
What you'll do
- 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
- Tracks regulatory submission timelines, deliverables, and health authority commitments
- Maintains current knowledge of applicable regulatory requirements and performs assigned activities in accordance with company procedures and applicable regulations
Pay
$84,400 – $99,300 a year
Employer providedThe pay range that the Company reasonably expects to pay for this headquarters-based position is $84,400 – $99,300; 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, CAHybridOpen 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 16, 2026
Salary intelligence
How the pay compares
This role's midpoint is level with the US median for Regulatory Affairs roles at this level.
This roleEmployer provided
Associate & Specialist roles in California14 roles publishing pay
Associate & Specialist roles in the US29 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $84,400 | — | $99,300 |
| California (middle half) | $87,875 | $91,750 | $95,375 |
| All US (middle half) | $78,000 | $91,500 | $95,000 |
This role: Corcept Therapeutics's own published range. Comparisons: the base pay employers published on open Regulatory Affairs roles at the same level on Regulatory Jobs, October 16, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Regulatory Affairs
The general path across 295 open Regulatory Affairs roles on Regulatory Jobs, with the titles they carry most. Not Corcept Therapeutics's own promotion track.
Career resources on Regulatory Affairs
Skills DNA
What this role leans on
How many of the posting's 25 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership10
- Regulatory submissions8
- Documentation and SOPs5
- Investigations and CAPA2
- GMP and compliance1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
From Regulatory News
Manufacturing and quality coverage for this professionCompany hiring pulse
Corcept Therapeutics on Regulatory Jobs
- 8
- Open roles
- 8
- Distinct roles
- 1
- Locations
By discipline
- Regulatory3 38%
- Quality3 38%
- Compliance & Safety2 25%
By level
- Manager3 38%
- Director2 25%
- Senior & Principal2 25%
More roles at Corcept Therapeutics
- View role
Associate Director, Regulatory Affairs
Redwood City, CA · HybridDirectorPharmaceuticals$215K–$253K
- View role
Quality Systems GxP Training Specialist II
Redwood City, CA · HybridSenior & PrincipalPharmaceuticals$106K–$125K
- View role
Manager, Computer Systems Validation (CSV)
Redwood City, CAManagerPharmaceuticals$161K–$189K
- View role
Senior Manager, Clinical Quality Assurance
Redwood City, CA · HybridManagerPharmaceuticals$173K–$204K
Similar Regulatory Affairs roles elsewhere
- View role
Regulatory Affairs Intern
Bristol Myers SquibbIndianapolis, INAssociate & SpecialistPharmaceuticals$50K–$94K
- View role
2027 Future Talent Program – Global Regulatory Affairs - Oncology – Co-op
MerckRahway, NJ · HybridAssociate & SpecialistPharmaceuticals$39K
Associate I, Regulatory Affairs at Corcept Therapeutics
Open until filled. $84K–$99K a year, employer provided.