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New · posted Oct 31

Corcept Therapeutics · Pharmaceuticals

Specialist I, Patient Safety and Pharmacovigilance Operations

  • Redwood City, CA
  • On-site
  • Full-time
  • Associate & Specialist
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EmploymentFull-time
DeadlineOpen 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.

This role supports Patient Safety and Pharmacovigilance (PSPV) Safety Operations activities in the postmarketing (PM) and clinical trial (CT) setting. The role is primarily responsible for the daily management of shared PSPV mailboxes and other safety intake channels, ensuring incoming communications are reviewed promptly, potential safety information is identified, and items are appropriately documented, routed, tracked, and escalated in accordance with established procedures and regulatory timelines.

What you need

Preferred Education and Experiencenice to have

  • Bachelor's degree in healthcare or life sciences degree such as RN or BSN, PharmD
  • 1+ years in healthcare setting, pharma or biotech company
  • Familiarity with global pharmacovigilance regulations and safety-reporting requirements is desirable

 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

  • Ability to work in a dynamic environment to meet patient and corporate needs
  • Excellent communication skills (verbal and written)
  • Ability to collaborate with cross-functional teams and support multiple projects in a fast-paced environment
  • Able to travel for up to 10% of time
  • Flexibility to be in office more than 3 days week to meet any business needs (e.g., audits, regulatory inspections)

What you'll do

  • Monitor and manage assigned PSPV shared mailboxes and intake channels, ensuring timely review and disposition of incoming reports and communications
  • Perform initial review/triage of incoming information to identify potential adverse events (AEs), serious adverse events (SAEs), product quality complaints (PQCs), special situations, and other safety-relevant information
  • Identify potential Individual Case Safety Reports (ICSRs) and ensure information is routed to the appropriate case-processing team or workflow within required timelines
  • Categorize, assign, route, file, and archive mailbox communications according to established procedures
  • Prioritize and escalate serious, urgent, medically significant, or time-sensitive safety information as required
  • Perform routine reconciliation of PSPV mailboxes and intake channels/sources to confirm potentially reportable information has been appropriately identified, received and processed
  • Support the development of training materials
  • Track and archive safety-related training for internal teams and vendors
  • Assist with audits, regulatory inspections, and inspection-readiness activities by providing intake records and supporting documentation, as needed
  • Perform additional PSPV projects and activities as assigned

Pay

$65,800 – $87,000 a year

Employer provided

The pay range that the Company reasonably expects to pay for this headquarters-based position is $65,800 – $87,000; 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)

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Equal 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 31, 2026

Salary intelligence

How the pay compares

This roleEmployer provided

$65,800 to $87,000 a year
Annual base pay
Annual base payLowMedianHigh
This role$65,800—$87,000

This role: Corcept Therapeutics's own published range.

Career trajectory

Where this role sits in Clinical Safety & Pharmacovigilance

The general path across 113 open Clinical Safety & Pharmacovigilance roles on Regulatory Jobs, with the titles they carry most. Not Corcept Therapeutics's own promotion track.

  1. This role

    Associate & Specialist

    Often: Associate, Pharmacovigilance Operations/Drug Safety · Clinical Sciences Partnership COE Coordinator

  2. Next step

    Senior & Principal

    Often: Senior Safety Scientist · Clinical FSP Quality Manager

    $186K median11 open
  3. Later

    Manager

    Often: Senior Manager, Clinical Quality Assurance · Clinical FSP Quality Manager

    $170K median15 open
  4. Later

    Director

    Often: Director · Senior Medical Director

    $260K median70 open
  5. Later

    VP & Executive

    Often: Head of Multiple Myeloma & AML, Oncology · Head of Patient-Facing Quality Assurance

    $347K median12 open

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.

GMP and compliance: 3 linesDocumentation and SOPs: 5 linesInvestigations and CAPA: 1 lineClinical trial conduct: 4 linesCollaboration and leadership: 9 linesGMPDocumentationInvestigationsClinical trialsTeamwork
  • Collaboration and leadership9
  • Documentation and SOPs5
  • Clinical trial conduct4
  • GMP and compliance3
  • Investigations and CAPA1

Company 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%
See all 22 Corcept Therapeutics roles

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Similar Clinical Safety & Pharmacovigilance roles elsewhere

Specialist I, Patient Safety and Pharmacovigilance Operations at Corcept Therapeutics

Open until filled. $66K–$87K a year, employer provided.

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