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Allergan

The Manager, Regulatory Affairs Submission Management, manages high impact, complex submission projects involving multiple cross-functional regulatory submission teams. With input from the submission ...

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As of Sep 13, 2026, the average hourly pay for associate regulatory submission manager in the United States is $32.21, according to ZipRecruiter salary data. Most workers in this role earn between $24.52 and $38.22 per hour, depending on experience, location, and employer.

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Infographic showing various Associate Regulatory Submission Manager job openings in the United States as of June 2026, with employment types broken down into 67% Full Time, 31% Part Time, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $66,992 per year, or $32.2 per hour.

Associate Director, Global Submission Management

Boston, MA • On-site

Vertex Pharmaceuticals
Biotechnology Research and Development • 1 - 5K employees
Learn more about Vertex Pharmaceuticalsexternal

$163K - $244K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 6 days ago

Vertex Pharmaceuticals rating

6.5

Company rating: 6.5 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

Job description

Job Description
General Summary:
The Associate Director, Global Submission Management (GSM) is responsible for the strategic oversight and execution of a portfolio of global regulatory submissions across development and lifecycle programs. This role will manage submissions for development-stage, lifecycle, regional, and post-approval, as well as supporting activities required to enable, maintain, and advance global product registrations. The disease area focus of this role will be Pulmonary or Cell & Gene Therapy.
This role ensures routine, regional, and lifecycle submissions are delivered efficiently, compliantly, and predictably in alignment with global regulatory strategies and operational objectives. This role partners closely with Major Submission Leads, Global Regulatory Strategy, Regulatory CMC, Labeling, Publishing, and Advertising & Promotion functions to support coordinated submission planning, execution consistency, and steady-state portfolio throughput.
Key Duties and Responsibilities:
  • Provides oversight for a defined portfolio of regulatory submissions, from planning through submission and closeout
  • Develops and maintains submission plans, timelines, and tracking across multiple programs
  • Ensures consistent application of submission management standards, tools, and processes
  • Partners with Global Regulatory Strategy, Regulatory CMC, Labeling, Publishing, and Advertising & Promotion to define submission scope, milestones, and deliverables
  • Coordinates cross-functional activities to ensure submission completeness, quality, and compliance
  • Identifies, manages, and resolves operational risks affecting submission timelines or quality
  • Oversees preparation of submission status updates, issue logs, and portfolio-level reporting
  • Supports workload planning and capacity management across the submission portfolio
  • Escalates risks appropriately when submissions approach higher-impact or higher-complexity thresholds
  • Leads, coaches, and supports submission management staff including vendor functional service providers (FSPs)
  • Contributes to continuous improvement, knowledge sharing, and talent development within submission management
  • Demonstrates the ability to effectively adopt and leverage emerging technologies, including AI driven tools, and maintains a continuous learning mindset to strengthen GSM decision-making and operational efficiency
  • Proactively remains up to date on advances in technology, AI, automation, competitive intelligence and changes in the Regulatory environment.

Knowledge and Skills:
  • Strong knowledge of global regulatory submission requirements, processes, and timelines
  • Experience with submission and project management tools and systems
  • Ability to manage multiple concurrent submissions and competing priorities
  • Strong organizational, planning, and problem-solving skills
  • Effective stakeholder management and cross-functional communication skills
  • Ability to drive execution consistency, compliance, and operational efficiency

Education and Experience:
  • Bachelor's degree in Life Sciences, Regulatory Affairs, Project Management, or a related discipline
  • 7+ years of experience in regulatory submission management, regulatory operations, or regulatory/clinical project management
  • Experience managing routine, regional, and lifecycle regulatory submissions across multiple regions
  • Experience working effectively in matrixed, cross-functional environments
  • People-management experience preferred
  • Experience using modern project management and regulatory submission tooling including MS Project, Smartsheet, and Veeva RIM
  • Experience managing submissions in Pulmonary or Cell & Gene Therapy is preferred

#LI-Hybid
At Vertex, we embrace continuous learning and encourage employees to stay informed on advances in AI, technology, automation, and industry trends. We seek talent who bring an external perspective, demonstrate curiosity and sound judgment, and thoughtfully adopt new capabilities that improve decision-making, drive innovation, increase efficiency, and help deliver better outcomes for patients.
Pay Range:
$163,200 - $244,800
Disclosure Statement:
The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.
At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.
Flex Designation:
Hybrid-Eligible Or On-Site Eligible
Flex Eligibility Status:
In this Hybrid-Eligible role, you can choose to be designated as:
1. Hybrid: work remotely up to two days per week; or select
2. On-Site: work five days per week on-site with ad hoc flexibility.
Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time.
#LI-Hybrid
Company Information
Vertex is a global biotechnology company that invests in scientific innovation.
Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com

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