Manager Regulatory Affairs Operations
Company | Acadia Pharmaceuticals |
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Location | Princeton, NJ, USA, San Diego, CA, USA |
Salary | $90000 – $112600 |
Type | Full-Time |
Degrees | Bachelor’s |
Experience Level | Senior |
Requirements
- Requires a Bachelor’s degree in Business Administration, Life Science discipline or related field.
- Targeting 5 years of experience in Regulatory Affairs Operations or relevant function.
- Working knowledge of eCTD guidances (e.g., ICH, FDA, EMA, etc.), requirements, and technologies.
- Knowledge, understanding, and experience with Veeva VAULT RIM authoring workflows, document metadata, and naming conventions.
- Strong working knowledge of tools and technologies related to document formatting/document-level publishing (e.g., Word, Acrobat, DXC Toolbox, authoring templates).
- Ability to work collaboratively with Regulatory Affairs, Medical Writing, and other functions to publish regulatory submissions and support management of documents and reports.
- Demonstrated ability to effectively communicate in written and verbal media concepts related to regulatory systems and electronic submissions.
- Ability to deliver while working under pressure to meet tight deadlines.
Responsibilities
- Using Acadia’s eCTD publishing (IQVIA RIM Smart) and document management (Veeva Vault RIM), publish eCTD submissions in alignment with health authority guidelines and industry best practices.
- For authored documents, provide guidance on formatting and review for adherence to Acadia’s Style Guide.
- Perform document verifications and follow procedures to identify, document, and communicate findings.
- Manage document management tasks including file transfer, storage, tracking, and archival services.
- Provide training to cross functional teams on Acadia style guide and Acadia authoring templates.
- Validate and QC published eCTD submissions, working collaboratively with teammates to resolve findings and issues.
- Support authors and contributors providing guidance on electronic document requirements to be included in regulatory submissions.
- Utilize Electronic Submission Gateway (ESG) to transmit submissions to FDA and other Health Authorities.
- Update trackers, correspondence logs, metrics on daily/weekly/monthly basis as internal policies dictate.
- Other activities as designated.
Preferred Qualifications
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No preferred qualifications provided.