Director, Major Application Submission Management

Job Description

The Director, Major Application Submission Management is accountable for the strategic oversight and execution of a defined portfolio of enterprise‑critical, major global regulatory applications across complex development and lifecycle programs. This role leads end‑to‑end submission planning and delivery for high‑impact filings, ensuring submissions are executed efficiently, compliantly, and in alignment with global regulatory and business strategies.

This role is scoped to major health authority applications (e.g., NDA, BLA, MAA, and equivalents) where submission outcomes have material regulatory, commercial, and patient‑access implications. The Director serves as a strategic partner to Global Regulatory Strategy, Regulatory CMC, Labeling, Publishing, and Advertising & Promotion functions, driving integrated submission plans, proactive risk management, and senior‑level decision support.

Key Duties & Responsibilities:

• Provides strategic leadership and oversight for submissions from planning through submission and closeout
• Drives development and execution of comprehensive submission plans, timelines, and portfolio‑level reporting
• Partners with Global Regulatory Strategy, Regulatory CMC, Labeling, Publishing, and Advertising & Promotion to define submission scope, milestones, deliverables, and dependencies
• Ensures alignment across cross‑functional teams and drives accountability for submission deliverables tied to major filings
• Leads identification, escalation, and mitigation of submission risks; develops contingency and scenario plans for complex programs
• Serves as senior escalation point for complex submission issues and drives resolution to completion
• Guides preparation of data‑driven analyses and reports to support resourcing, prioritization, and trade‑off decisions
• Communicates submission progress, risks, and outcomes clearly to senior leadership and governance bodies

Knowledge and Skills:

• Expertise in global regulatory submission planning and execution
• Strong knowledge of health authority submission requirements, guidelines, and timelines
• Experience with submission and project management tools and systems
• Strong stakeholder management, influence, and change‑management skills
• Demonstrated ability to manage multiple complex priorities and drive firm deadlines
• Excellent written and verbal communication skills with the ability to engage senior leadership
• Strong organizational, analytical, and problem‑solving capabilities

Education and Experience Level:

• Bachelor's degree and/or Advanced degree in Life Sciences, Regulatory Affairs, Project Management, or a related discipline.
• 10+ years' experience in regulatory submission management, regulatory operations, or regulatory/clinical project management
• Demonstrated experience leading major global regulatory applications (e.g., NDA, BLA, MAA or equivalents)
• Proven people‑management experience and ability to lead high‑performing teams
• Experience operating in highly matrixed, cross‑functional environments

#LI-TC1

#LI-Hybrid

Pay Range:

$190,400 - $285,600

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