Regulatory Strategy Associate Director

Job Description

General Summary:

The Regulatory Strategy Associate Director will be responsible for overseeing the development of regional or global regulatory strategy for development programs or marketed products. This role will serve as a global regulatory lead or in some cases a regional regulatory lead for development and/or commercial product(s) within the Vertex portfolio and contribute to the global regulatory strategy for the assigned program(s). This role requires advanced understanding of regulatory affairs frameworks in the US Europe or other international markets drug development and related concepts and the ability to translate this knowledge into effective regulatory planning and strategy development.

Key Duties and Responsibilities:

• Lead the development and implementation of global regulatory strategy for assigned projects in development through commercial stages
• Contributes to and may lead the development and implementation of regional regulatory strategy to inform the global strategy for certain projects
• Leads regulatory communications and interactions with health authorities
• Advises teams on regulatory requirements for development and approval pathways including potential for expedited pathways
• Leads and oversees the process for preparation submission and approval of regulatory applications
• Provides strategic and technical regulatory input for key product development or registration documents
• Ensures compliance of regulatory submissions with current regulations and guidance
• Reviews and evaluates regulatory intelligence and guidance information to continuously inform regulatory strategy
• Advises cross-functional teams and senior management on regulatory risks considerations and strategies for program(s)
• Acts as an advisor and coach to mentor members of the team

Knowledge and Skills:

• Specialized knowledge of global and regional regulatory affairs frameworks and guidelines Understanding of requirements and processes to maintain a product on the market; reporting and surveillance
• Comprehensive understanding of drug development and related concepts such as clinical trial design statistics and clinical pharmacology
• Comprehensive understanding of requirements and processes to maintain a product on the market product labeling reporting and surveillance
• Ability to assess and understand complex scientific information regulatory precedent competitive intelligence and regulatory guidelines and make recommendations based on assessment
• Strong problem-solving skills
• Demonstrates the ability to effectively adopt and leverage emerging technologies including AI-driven tools and maintains a continuous learning mindset to strengthen regulatory strategy decision-making and operational efficiency.
• Proactively remains up to date on advances with technology AI automation competitive intelligence and changes in the regulatory environment.
• Strong written and verbal communication skills tailored to multiple audiences to communicate difficult concepts and persuade others to adopt a different point of view
• Ability to effectively lead and work within a team environment
• Prior experience with major health authority submissions and health authority interactions is required.

Education and Experience:

• Bachelors degree in biology Chemistry or other related discipline
• Typically requires 8 years of relevant pharmaceutical or biotech industry experience within regulatory affairs or the equivalent combination of education and experience

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Pay Range:

Disclosure Statement:

Flex Designation:

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 Vertexs Policy on Flex @ Vertex Program and may be changed at any time.

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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 persons 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