Vertex Pharmaceuticals Inc (US) Posted November 11, 2026

Associate Director, Regulatory Technology

Boston, United States Full time
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Vertex Pharmaceuticals Inc (US) is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Job Description

The Associate Director, Regulatory Technology is accountable for translating Regulatory priorities into an actionable technology roadmap across Regulatory-owned platforms. The role owns demand intake, prioritization, release planning, and enhancement delivery; serves as the primary business liaison to Digital Technology and Engineering (DTE) teams; and advances Regulatory capabilities through AI, automation, and emerging technologies. Working across Regulatory, DTE, and business stakeholders, the Associate Director helps ensure technology investments are aligned, scalable, compliant, and positioned to deliver measurable business value.

Key Duties and Responsibilities:

Maintain the Regulatory Technology roadmap across Regulatory-owned platforms, aligning planned capabilities and investments with Regulatory priorities and the broader technology strategy.

Lead the end-to-end demand intake and prioritization process, partnering with business stakeholders to define needs, assess value, dependencies, risk, and readiness, and establish a transparent delivery sequence.

Drive release planning and enhancement delivery across the platform portfolio, coordinating scope, business requirements, timelines, testing readiness, communications, and adoption activities with product owners and delivery teams.

Serve as the primary Regulatory business liaison to DTE teams, translating business needs into clear technology requirements and facilitating timely decisions, issue resolution, and alignment across functions.

Establish and facilitate appropriate roadmap and portfolio governance, providing clear visibility to priorities, delivery status, risks, dependencies, decisions, and expected outcomes.

Drive innovation through AI, automation, and emerging technologies by identifying high-value opportunities, shaping pilots, defining success measures, and advancing viable concepts toward scalable solutions.

Partner with Regulatory process owners, data and technology teams, and end users to ensure solutions support compliant, efficient, and user-centered ways of working.

Monitor regulatory technology trends, industry practices, and evolving business needs to inform roadmap choices and recommend future capabilities.

Support change management and adoption by developing stakeholder engagement, communications, training, and feedback approaches appropriate to each release or initiative.

Communicate roadmap progress, delivery outcomes, risks, and recommendations to Regulatory leadership and cross-functional stakeholders.

Required Education Level

Bachelor's degree in life sciences, information technology, engineering, business, or a related field.

Required Experience

Typically requires 8 years of relevant experience in regulatory technology, regulatory operations, product management, business technology, or a related area within the pharmaceutical or biotechnology industry, or the equivalent combination of education and experience.

Demonstrated experience managing technology roadmaps, demand intake, prioritization, release planning, and enhancement delivery across a portfolio of business platforms.

Experience partnering with enterprise technology teams and cross-functional business stakeholders to deliver technology-enabled capabilities in a regulated environmen.

Experience evaluating or implementing AI, automation, or other emerging technologies, including pilots and scale-up planning.

Required Knowlede/Skills

Strong product and portfolio management capabilities, including roadmap development, demand management, prioritization, release planning, and value realization.

Working knowledge of Regulatory Affairs and Regulatory Operations processes, data, content, and technology within the pharmaceutical or biotechnology industry.

Strong technical expertise in Veeva Vault RIM and integrations across the Veeva suite, including Veeva Quality, Clinical, and PromoMats.

Ability to translate business needs into clear, outcome-focused requirements and to communicate effectively with both business and technical audiences.

Strong stakeholder management, facilitation, influencing, and decision-making skills across organizational levels and functions.

Demonstrated ability to manage multiple initiatives, dependencies, risks, and competing priorities in a complex environment.

Knowledge of technology governance, software delivery practices, system lifecycle considerations, and compliance expectations for regulated platforms.

Ability to identify practical applications for AI, automation, and emerging technologies while considering scalability, adoption, risk, and business value.

Strong analytical, problem-solving, communication, and change management skills.

Ability to work independently, exercise sound judgment, and lead through influence in a matrixed organization.

Other Requirements

Ability to engage with global stakeholders across time zones as business needs require.

Travel may be required based on business needs.

#LI-Hybrid

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:

$164,000 - $246,000

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

Job details

Seniority
Associate Director
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Boston, United States
Employment type
Full time

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 279 comparable Associate Director Regulatory Affairs roles across 84 biopharma companies.

279Comparable roles tracked
257Currently active
84Companies hiring similar roles
35Countries represented

Salary context

74 of 279 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject $164,000/yr – $246,000/yr
Peer group range $123,250 – $236,300 (median $180,500)

Where these roles are based

Top locations among the 279 comparable roles

United States116
India29
Japan20
United Kingdom19
Ireland12
Poland9

+ 29 more countries

Seniority mix

279 of 279 peers have a known seniority level

Manager168
Senior59
Associate Director52

Therapeutic area mix

29 of 279 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Immunology13
Oncology9
Ophthalmology4
Dermatology & Aesthetics1
Rare Disease1
Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Celgene - Summit (Corp) Princeton, United States Associate Director
Same function Same seniority Same country
60%similar
Merck KGaA Billerica, Massachusetts, United States Associate Director
Same function Same seniority Same country
60%similar
ModernaTX, Inc. Cambridge, United States Associate Director
Same function Same seniority Same country
60%similar
ModernaTX, Inc. Cambridge, United States Associate Director
Same function Same seniority Same country
60%similar
Vertex Pharmaceuticals Inc (US) Boston, United States Associate Director
Same function Same seniority Same country
60%similar
Neurocrine Biosciences Inc. US CA San Diego, United States Associate Director
Same function Same seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Regulatory Affairs job in the United States, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Associate Director, Global Regulatory Sciences - CMC
Celgene - Summit (Corp) · Princeton, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, Global Regulatory Advertising and Promotion
ModernaTX, Inc. · Cambridge, United States · Associate Director
Function Therapeutic area Seniority Country
60%
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Regeneron Pharmaceuticals, Inc (USA) · Warren, United States · Associate Director
Function Therapeutic area Seniority Country
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Associate Director, Regulatory Affairs Advertising & Promotion - Oncology
AbbVie · Florham Park, NJ · Associate Director
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.