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Director, Pharmacovigilance Operations and Engagement

Job in Redwood City, San Mateo County, California, 94061, USA
Listing for: Corcept Therapeutics
Part Time position
Listed on 2026-02-08
Job specializations:
  • Healthcare
    Healthcare Management, Healthcare Administration
Salary/Wage Range or Industry Benchmark: 125000 - 150000 USD Yearly USD 125000.00 150000.00 YEAR
Job Description & How to Apply Below

Corcept is leading the way in the research and development of cortisol modulators, molecules that regulate cortisol activity at the glucocorticoid receptor (GR). To date, we have discovered more than 1,000 selective proprietary cortisol modulators. In 2012, we received FDA approval of Korlym® (mifepristone), the first approved treatment for hypercortisolism (Cushing’s syndrome). Today, our team and collaborators continue to unlock the possibilities of cortisol modulation as a way to treat serious diseases, with more than 30 ongoing studies across endocrinology, oncology, metabolism, and neurology.

We remain dedicated to advancing the possibilities of cortisol modulation.

Overview

This role serves as the PSPV lead for cross-functional activities and commercial initiatives, ensuring successful product launch and lifecycle management with patient safety integrated throughout the organization. This highly visible role acts as a strategic partner to Medical Affairs, Quality, Legal, and Commercial teams, driving operational and compliance excellence across all touchpoints. This is a hybrid role typically requiring on-site presence at least 3 days per week at company headquarters in Redwood City.

Responsibilities
  • Cross-Functional Leadership &

    Collaboration:

    Build strategic partnerships and alignment of patient safety objectives and deliverables with internal stakeholders (Medical Affairs, Quality, Legal, Commercial) and external vendors/partners
  • Establish and lead cross functional governance forum with PSPV, Medical Affairs, Quality, Legal, Commercial to review all commercial initiatives/activities for cross functional planning and execution
  • Act as the Safety Lead for implementation and oversight of call center and commercial programs (e.g., specialty pharmacies, patient support programs, market research, distributors, etc.) including:
    • Reviewing vendor contracts and program materials to ensure inclusion of safety-related reporting requirements and deliverables
    • Ensuring appropriate systems and processes are in place for reporting safety information to Corcept in compliance with contractual obligations and global reporting timelines
    • Developing and coordinating adverse event reporting training
    • Overseeing reconciliation processes between vendors and internal PV systems to ensure completeness and accuracy of safety data
    • Ensuring appropriate quality controls are in place for the call center and commercial programs, including source data verification and quality sampling of safety data
    • Maintaining tracking of vendors/providers for the pharmacovigilance system master file
    • Collaborate closely with Medical Affairs to integrate key safety messages into scientific communications and materials
Compliance & Quality Oversight
  • Contribute to review of deviations and CAPAs for commercial programs and call center
  • Monitor and report compliance key performance indicators for commercial programs and call center to PSPV compliance lead
  • Support audit and inspection readiness, including being the PSPV SME for commercial programs and call center activities
Strategic Planning & Process Optimization
  • Identify opportunities for process improvements and technology solutions to enhance PV systems and workflows
  • Stay current with evolving global PV regulations and assess impact on organizational practices
  • Support development of PV strategies aligned with corporate objectives and patient safety goals
Preferred Skills, Qualifications and Technical Proficiencies
  • Ability to work in a dynamic environment to meet patient and corporate needs
  • Deep knowledge of global PV regulations (ICH, GVP, FDA, EMA)
  • Proven ability to lead cross-functional teams and influence commercial strategies
  • Ability to manage multiple projects in a fast-paced environment
  • Excellent communication (written and verbal) and stakeholder management skills
  • Proficiency in safety database systems (e.g., Argus) and electronic reporting requirements
  • Able to travel for up to 10% of time
Preferred

Education and Experience
  • Degree in Healthcare or Life Sciences; advanced degree preferred
  • 10+ years in pharmacovigilance biopharma
  • 5+ years in leadership roles with cross-functional and commercial exposure
  • Experience…
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