Senior Manager, Commercial Regulatory Operations
Corcept Therapeutics
June 24, 2026
Remote friendly (Redwood City, CA)
United States
Operations
Responsibilities:
- Manage the end-to-end content review and approval process for promotional and non-promotional materials using the Veeva document management system.
- Drive process improvement and operational efficiency initiatives within the CRT workflow.
- Support system maintenance and enhancements in Veeva PromoMats and MedComms (administrative updates and light configuration changes).
- Partner with Marketing teams to develop and maintain claims and reference libraries.
- Collaborate with Regulatory, Medical, and Legal to maintain CRT workflows for review and approval of product/disease-related content proposed by Marketing, Medical Affairs, and agencies.
- Lead planning and facilitation of CRT meetings (agenda, calendar coordination, expedited review processing, quality checks, consensus documentation).
- In partnership with Regulatory colleagues, prepare timely and accurate FDA Form 2253 submissions.
- Monitor and report on approval metrics.
- Support prioritization and capacity planning aligned to business objectives and key timelines.
- Provide onboarding and training for CRT reviewers and content creators on CRT processes, system navigation, and best practices.
- Provide project oversight and vendor management for Veeva system enhancements and upgrades.
Preferred Skills/Qualifications/Technical Proficiencies:
- Expertise in Veeva PromoMats/MedComms and promotional/non-promotional material review processes.
- Ability to manage without direct authority and influence effectively.
- Excellent analytical, problem-solving, and communication skills.
- Highly organized, detail-oriented, adaptable.
Preferred Education/Experience:
- BA/BS in health/life sciences or related field.
- 6+ years in pharma/life sciences (including leading or supporting review committee meetings).
- Product launch and pre-approval commercialization experience.
- Experience in AI implementation, claims library maintenance, and Veeva administrative support.
Application Instructions:
- Applicants must be currently authorized to work in the United States on a full-time basis.
- Manage the end-to-end content review and approval process for promotional and non-promotional materials using the Veeva document management system.
- Drive process improvement and operational efficiency initiatives within the CRT workflow.
- Support system maintenance and enhancements in Veeva PromoMats and MedComms (administrative updates and light configuration changes).
- Partner with Marketing teams to develop and maintain claims and reference libraries.
- Collaborate with Regulatory, Medical, and Legal to maintain CRT workflows for review and approval of product/disease-related content proposed by Marketing, Medical Affairs, and agencies.
- Lead planning and facilitation of CRT meetings (agenda, calendar coordination, expedited review processing, quality checks, consensus documentation).
- In partnership with Regulatory colleagues, prepare timely and accurate FDA Form 2253 submissions.
- Monitor and report on approval metrics.
- Support prioritization and capacity planning aligned to business objectives and key timelines.
- Provide onboarding and training for CRT reviewers and content creators on CRT processes, system navigation, and best practices.
- Provide project oversight and vendor management for Veeva system enhancements and upgrades.
Preferred Skills/Qualifications/Technical Proficiencies:
- Expertise in Veeva PromoMats/MedComms and promotional/non-promotional material review processes.
- Ability to manage without direct authority and influence effectively.
- Excellent analytical, problem-solving, and communication skills.
- Highly organized, detail-oriented, adaptable.
Preferred Education/Experience:
- BA/BS in health/life sciences or related field.
- 6+ years in pharma/life sciences (including leading or supporting review committee meetings).
- Product launch and pre-approval commercialization experience.
- Experience in AI implementation, claims library maintenance, and Veeva administrative support.
Application Instructions:
- Applicants must be currently authorized to work in the United States on a full-time basis.