Remote Position

[Remote] Manager, Regulatory Operations and Publishing

🌍 Remote Β· United States πŸ’Ό Full-time

Note: The job is a remote job and is open to candidates in USA. RayzeBio, a wholly-owned subsidiary of Bristol Myers Squibb, is hiring a Manager, Regulatory Operations and Publishing to manage regulatory submission operations and publishing. The role oversees document formatting, PDF publishing, technical quality control, submission execution, vendor coordination, and regulatory operations processes.

Responsibilities

  • Manage day-to-day regulatory submission operations activities to ensure high-quality, timely, and compliant health authority submissions
  • Format complex documents according to company formatting standards to optimize PDF rendering and limit manual publishing of PDF documents
  • Generate submission-ready PDFs in compliance with regulatory guidance, eCTD requirements, and internal PDF publishing standards
  • Perform technical QC of submission documents and published submissions to ensure accuracy, consistency, completeness, and compliance with submission requirements
  • Manage submission execution activities, including deliverable tracking, timeline coordination, submission readiness assessments, and communication with Regulatory Affairs and cross-functional stakeholders to ensure timely submission delivery
  • Coordinate with external submission vendors to support timely and high-quality submission delivery
  • Provide technical support to authoring teams on the use of StartingPoint templates
  • Support reference management activities, including maintaining references in EndNote or other reference management tools
  • Partner with Regulatory Affairs, Clinical, Nonclinical, CMC, Medical Writing, Quality, and external vendors to resolve formatting, publishing, and QC issues
  • Support creation and maintenance of data, records, and documents in Veeva Vault RIM and other systems, as applicable
  • Support development and continuous improvement of Regulatory Operations SOPs, work instructions, templates, checklists, and submission standards
  • Maintain current knowledge of FDA, ICH, and other applicable regulatory requirements related to electronic submissions and document standards

Skills

  • Bachelor's degree with 4+ years of Regulatory Operations experience
  • Demonstrated expertise in Microsoft Word formatting, PDF publishing, and submission document preparation
  • Strong understanding of eCTD submission structure, PDF specifications, bookmarks, hyperlinks, file naming, and submission-ready document standards
  • Experience performing technical quality control of regulatory submissions and published eCTD sequences
  • Highly detail-oriented, with strong focus on accuracy, consistency, and quality
  • Strong organizational skills, with the ability to manage multiple concurrent submissions and competing priorities
  • Ability to troubleshoot complex document formatting and PDF publishing issues
  • Ability to work independently and follow tasks through from start to finish
  • Strong communication and interpersonal skills
  • Ability to collaborate effectively with internal teams and external vendors
  • Proactive, professional, and confident
  • Excellent professional ethics and integrity
  • Experience with Accenture StartingPoint Templates and Veeva RIM preferred

Benefits

  • Wellbeing support, retirement and financial protection benefits, and medical, dental, vision, life and disability insurance offerings, subject to the terms and conditions of the applicable plans and eligibility.
  • For U.S.-based exempt employees: Flexible Time Off (FTO), providing paid time off without a set accrual limit, subject to manager approval, and 11 paid company holidays each year.
  • For RayzeBio employees: 160 hours of paid vacation annually for new hires, subject to manager approval; 11 paid company holidays; and 3 optional holidays.
  • Depending on eligibility: paid sick leave; up to two paid volunteer days per year; summer hours flexibility; and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs.
  • For eligible employees: an annual Global Shutdown between Christmas Day and New Year's Day.
  • Remote work.

Company Overview

  • At Bristol Myers Squibb, we work every day to transform patients’ lives through science. It was founded in 1887, and is headquartered in New York, New York, USA, with a workforce of 10001+ employees. Its website is http://www.bms.com.
  • Company H1B Sponsorship

  • Bristol Myers Squibb has a track record of offering H1B sponsorships, with 189 in 2026, 247 in 2025, 278 in 2024, 231 in 2023, 180 in 2022, 181 in 2021, 169 in 2020. Please note that this does not guarantee sponsorship for this specific role.
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