Jobs · Manufacturing · California

Senior Director, Regulatory Operations

Acadia Pharmaceuticals · San Diego, CA · 6 days ago
HybridManufacturingFull-time

Position Summary

Lead and scale the global Regulatory Operations function, including organizational design, talent strategy, and performance management aligned to business and regulatory objectives.

Primary Responsibilities

  • Provide strategic oversight of electronic submission publishing, regulatory information management, and submission management across global health authorities.
  • Direct worldwide eCTD and non-eCTD electronic submissions to ensure compliance with health authority, ICH, and global regulatory standards.
  • Drive evaluation, implementation, and optimization of regulatory systems and tools, including Veeva Vault RIM and publishing platforms, ensuring validated, compliant, and scalable solutions.
  • Champion digital transformation initiatives within Regulatory Affairs, including the application of AI and advanced analytics to enhance submission readiness and operational insights.
  • Partner with IT, Quality, and cross-functional stakeholders to define system requirements, oversee validation, manage upgrades, and support evolving regulatory needs.
  • Establish and maintain work instructions, training programs, and quality control processes to ensure submission accuracy, consistency, and inspection readiness.
  • Ensure compliance with global regulatory technical standards, including eCTD, CDISC, and SEND, and lead adoption of evolving industry best practices.
  • Other duties as assigned.

Education/Experience/Skills

  • Bachelor’s degree in life sciences or a related field
  • Minimum of 12 years of progressively responsible experience in Regulatory Operations or Regulatory Affairs
  • Minimum of 8 years of leadership experience with responsibility for electronic submissions, regulatory systems, and submission management
  • Hands-on expertise with regulatory information management and publishing systems, including Veeva Vault RIM and eCTD tools
  • Experience overseeing validated regulatory systems and understanding of the software development lifecycle
  • Willingness and ability to travel domestically and internationally

Physical Requirements

  • Regular standing, walking, sitting, and the use of hands for handling or operating equipment
  • Occasional lifting and/or moving up to 20 pounds
  • Able to communicate visually, verbally, and audibly in a standard office environment and while working independently from remote locations

What we offer US-based Employees

  • Competitive base, bonus, new hire and ongoing equity packages
  • Medical, dental, and vision insurance
  • Employer-paid life, disability, business travel and EAP coverage
  • 401(k) Plan with a fully vested company match 1:1 up to 5%
  • Employee Stock Purchase Plan with a 2-year purchase price lock-in
  • 15+ vacation days
  • 13 -15 paid holidays, including office closure between December 24th and January 1st
  • 10 days of paid sick time
  • Paid parental leave benefit
  • Tuition assistance

EEO Statement (US-based Employees)

We are committed to building a diverse, equitable, inclusive, and innovative company, and we are looking for the BEST candidate for the job. That candidate may be one who comes from a less traditional background or may meet the qualifications in a different way.

Additional Information

Please note that reasonable accommodations granted throughout the recruiting process are not guaranteed to be the same accommodations given if hired. A new request will need to be submitted for any ADA accommodations after starting employment.

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