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 Safety Science Associate Director will report to the Head of Safety Science and is responsible for safety monitoring of assigned Corcept products (investigational and marketed), with core safety deliverables related to safety governance, signal detection/management, periodic and aggregate reporting. This role serves as an independent Safety Science contributor and collaborates with safety physicians and cross-functional stakeholders to support product development and lifecycle management activities.

Responsibilities:

Safety Data Analysis & Signal Detection:

Perform safety data analyses using appropriate data sources, including case series reviews, data summaries and AE trend information
Collaborate with safety physicians on signal detection and risk management activities. Perform safety data monitoring, analysis, and interpretation
Review of medical and scientific literature for signal detection and aggregate reporting activities

Safety Documentation & Reporting:

Develop and maintain components of Risk Management Plans (RMPs)/Risk Evaluation and Mitigation Strategies (REMS), and other risk management documents for assigned product(s)
Prepare and review aggregate safety reports for assigned product(s)
Provide safety input to statistical analysis plans, data analysis visualizations, and documents requiring safety analysis to ensure consistent presentation of safety and risk management topics for assigned product(s)
Author and review safety reports and regulatory deliverables, including Integrated Summaries of Safety (ISS) and other submission-related documents

Cross-Functional Collaboration:

Participate in safety governance meetings and support safety deliverables related to cross functional or benefit-risk assessment meetings, including creation and maintenance of product core safety information and company core data sheets (CCDSs)
Contribute to and review safety sections of clinical documents, including Investigator’s brochure (IB), clinical study protocols, and clinical study reports

Regulatory & External Engagement:

Work closely with safety physicians and cross-functional stakeholders in authoring the safety safety content for regulatory submissions and other key regulatory deliverables (e.g., NDA, Briefing Document)
Prepare and review responses to health authority or other safety related query responses for assigned product(s)

Leadership & Team Development:

Mentor, train and collaborate with junior scientists on signal detection and risk management activities
Support PV vendor oversight and continuous process improvement

Preferred Skills, Qualifications and Technical Proficiencies:

Ability to work in a dynamic environment to meet corporate and patient needs
Excellent working knowledge of Argus (or similar applications), MS Office applications, electronic data capture systems, and MedDRA and WHO Drug coding dictionaries
Excellent presentation, communication, and collaboration skills
Knowledge of global PV regulations and guidelines (e.g., ICH, GVP, FDA, EMA)

Preferred Education and Experience:

PhD, PharmD or other advanced degree in related discipline is preferred. Other relevant experience may be considered without an advanced degree; BS/BA degree in related discipline is required. Training or equivalent experience in epidemiology or public health is beneficial but not required
4+ years in experience in patient safety and pharmacovigilance in the capacity of a scientist, including experience in safety surveillance, signal detection and evaluation, aggregate reporting, and risk management activities. At least 2 years of clinical development experience is required
Experience in writing safety analyses, performing signal detection or safety surveillance, risk management and preparing responses to HA
Authoring and review of periodic and ad hoc safety reports and clinical development documents, including PSURs/PBRERs, DSURs, Clinical Overviews, Clinical Study Reports, Investigator's Brochures, or related documents
Experience with industry standard pharmacovigilance data systems (e.g., Oracle Argus, data analytics, and signal management tools)
Experience with NDA/MAA filing is beneficial but not required

The pay range that the Company reasonably expects to pay for this headquarters-based position is $183,500 - $269,800; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

Applicants must be currently authorized to work in the United States on a full-time basis.

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.

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.

Please visit our website at: https://www.corcept.com/

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.