
New · posted Oct 31
Corcept Therapeutics · Pharmaceuticals
Senior Medical Director, Therapeutic Area Safety Physician - Oncology and Neurology
- Redwood City, CA
- On-site
- Full-time
- Director
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 Medical Director, Therapeutic Area Safety Physician provides senior medical safety leadership within assigned therapeutic areas for clinical development program(s) and, as applicable, post-marketing pharmacovigilance activities. Reporting to the Lead Medical Safety Physician, this role provides strategic medical oversight of safety surveillance, safety analyses, emerging safety issues, and benefit–risk assessment.
The role partners closely with Safety Science, Clinical Development, Medical Affairs, Regulatory, Safety Operations, and Medical Review to ensure integrated, medically sound assessment of safety information and appropriate incorporation of safety considerations into development and lifecycle decisions. The role serves as a senior medical safety leader for assigned therapeutic areas and programs, providing medical leadership for safety strategy, benefit-risk assessment, governance activities, and cross-functional decision-making throughout the product lifecycle.
What you need
Preferred Education and Experiencenice to have
- MD or equivalent medical degree required; board certification preferred
- 10+ years of relevant experience in the biotechnology or pharmaceutical industry, including substantial experience in pharmacovigilance, drug safety, or medical safety
- Extensive experience providing strategic medical safety oversight across clinical development and/or post-marketing programs
- Strong experience in medical case review, signal evaluation, safety surveillance, and benefit–risk assessment
- Demonstrated experience providing medical safety leadership within one or more therapeutic areas and working with cross-functional development teams
- Demonstrated experience supporting NDA and/or MAA filings, including development of safety content and responses to regulatory questions
- Strong understanding of global pharmacovigilance regulations and safety requirements
- Experience contributing to regulatory submissions and health authority interactions
- Demonstrated leadership, mentoring, and/or people management experience
- Ability to exercise independent medical judgment while operating effectively within a highly collaborative, matrixed organization
- Experience in a growing biotechnology or pharmaceutical organization preferred
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
- Therapeutic area medical safety leadership
- Strong clinical and scientific judgment
- Benefit-risk and medical decision-making
- Signal evaluation and safety surveillance
- Cross-functional influence and collaboration
- Strategic thinking and execution
- Leadership, mentoring, and talent development
- Clear, concise, and effective communication
- Ability to operate effectively in a fast-paced, evolving environment
What you'll do
Therapeutic Area Medical Safety Leadership
- Serve as the senior Medical Safety Physician for assigned therapeutic areas, providing medical safety leadership across clinical development and post-marketing activities
- Develop and execute medical safety strategies aligned with program development plans, product lifecycle objectives, and applicable regulatory requirements
- Provide independent medical assessment of emerging safety information, potential risks, and evolving benefit–risk considerations
- Identify and proactively communicate important safety issues, trends, and emerging risks to appropriate governance bodies and senior leadership
- Ensure appropriate escalation of significant or potentially significant safety concerns to the Lead Medical Safety Physician and relevant safety governance forums
Signal Evaluation & Surveillance
- Lead or contribute to signal detection, validation, evaluation, and ongoing safety surveillance for assigned products and therapeutic areas in partnership with Safety Science
- Evaluate cumulative and emerging safety data from clinical trials, post-marketing sources, literature, epidemiologic data, and other relevant sources
- Provide medical input into safety topics, emerging risks, and potential signals, including assessment of clinical relevance and implications for patient safety
- Ensure appropriate documentation and communication of medical safety conclusions and recommendations
Benefit–Risk Assessment & Risk Management
- Lead medical safety input into ongoing benefit–risk assessments for assigned programs
- Provide safety expertise for development decisions, including protocol design, eligibility criteria, monitoring strategies, dose selection, and risk mitigation approaches
- Provide medical safety input into Risk Management Plans, risk minimization strategies, safety specifications, and other risk-management activities as applicable
- Ensure safety risks and mitigation strategies are appropriately reflected in protocols, Investigator’s Brochures, Clinical Study Reports, regulatory submissions, and other relevant documents
Cross-Functional Therapeutic Area Leadership
- Serve as the primary Medical Safety Physician partner to Clinical Development Therapeutic Area Medical Leads for assigned programs
- Establish strong, constructive partnerships with Clinical Development, Medical Affairs, Regulatory, Clinical Operations, Biostatistics, Data Management, and other functions
- Integrate safety insights into broader therapeutic area and asset strategies while maintaining independent medical safety judgment
- Represent Medical Safety in program team meetings, development governance forums, and cross-functional decision-making
- Partner with Medical Affairs to support medically accurate and consistent safety communication across internal and external materials
Regulatory & Safety Governance
- Provide medical safety leadership and input into DSURs, PADERs/PBRERs, Clinical Evaluation Reports, safety sections of regulatory submissions, and other aggregate safety reports
- Provide medical input for responses to health authority safety questions and participate in regulatory interactions as appropriate
- Provide medical safety leadership within product- or program-level safety governance activities, including evaluation of emerging safety issues, benefit-risk assessments, and safety-related development decisions
- Ensure safety decisions are appropriately documented, supported by available evidence, and escalated when necessary
- Support inspection and audit readiness and participate in health authority inspections or audits as appropriate
Organization Leadership
- Provide leadership, coaching, and mentoring to Medical Safety Physicians and other safety professionals
- Where applicable, directly manage Medical Safety Physicians and contribute to performance management, talent development, and succession planning
- Serve as a senior medical safety resource and subject matter expert
- Contribute to the development and implementation of Medical Safety standards, operating procedures, training programs, and quality initiatives
- Promote consistency and high-quality medical safety practices across therapeutic areas while identifying opportunities for continuous improvement
- Partner with the Lead Medical Safety Physician on organizational scaling, resource planning, capability development, and strategic priorities
Pay
$298,000 – $350,600 a year
Employer providedThe pay range that the Company reasonably expects to pay for this headquarters-based position is $298,000- $350,600; 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 · November 3, 2026
Salary intelligence
How the pay compares
This role's midpoint is 23% above the US median for Clinical Safety & Pharmacovigilance roles at this level.
This roleEmployer provided
Director roles in California19 roles publishing pay
Director roles in the US87 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $298,000 | — | $350,600 |
| California (middle half) | $234,000 | $264,000 | $294,500 |
| All US (middle half) | $221,250 | $263,500 | $279,250 |
This role: Corcept Therapeutics's own published range. Comparisons: the base pay employers published on open Clinical Safety & Pharmacovigilance roles at the same level on Regulatory Jobs, November 3, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Safety & Pharmacovigilance
The general path across 161 open Clinical Safety & Pharmacovigilance roles on Regulatory Jobs, with the titles they carry most. Not Corcept Therapeutics's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 62 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership27
- Clinical trial conduct10
- Quality systems and risk8
- Regulatory submissions6
- Documentation and SOPs5
- GMP and compliance2
- Investigations and CAPA1
- Validation and qualification1
- Data and digital systems1
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
- 22
- Open roles
- 22
- Distinct roles
- 1
- Locations
By discipline
- Clinical17 77%
- Regulatory3 14%
- Quality2 9%
By level
- Director10 45%
- Senior & Principal5 23%
- Manager4 18%
More roles at Corcept Therapeutics
- View role
Senior Director, Clinical Trial Patient Safety Lead
Redwood City, CADirectorPharmaceuticals$238K–$316K
- View role
Associate Director, Patient Safety & Pharmacovigilance Science
Redwood City, CADirectorPharmaceuticals$184K–$270K
- View role
Senior Specialist I, Patient Safety & Pharmacovigilance (Clinical Trial Safety Operations)
Redwood City, CASenior & PrincipalPharmaceuticals$104K–$137K
- View role
Specialist I, Patient Safety and Pharmacovigilance Operations
Redwood City, CAAssociate & SpecialistPharmaceuticals$66K–$87K
Similar Clinical Safety & Pharmacovigilance roles elsewhere
- View role
Associate Director, Pharmacovigilance- FSP
Thermo Fisher ScientificChapel Hill, NCDirectorPharmaceuticalsSalary not listed
- View role
Sr. Principal Scientist (Sr. Director), Drug Safety
MerckNorth Wales, PA +1 more · HybridDirectorPharmaceuticals$210K–$331K
- View role
Associate Director, Patient Safety Scientist
Bristol Myers SquibbMadison, NJ +1 moreDirectorPharmaceuticals$150K–$182K
- View role
Medical Director, Senior Patient Safety Physician
AstraZenecaCambridge, MA · HybridDirectorPharmaceuticals$250K–$375K
Senior Medical Director, Therapeutic Area Safety Physician - Oncology and Neurology at Corcept Therapeutics
Open until filled. $298K–$351K a year, employer provided.

