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Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Associate Director - Regulatory Technology

Enterprise ApplicationsPosted on Nov 11
Full-timeBoston, MA, USA

About the Job

Requirements

  • A bachelor's degree in life sciences, information technology, engineering, business, or a related field is required.
  • 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 an 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 environment.
  • Experience evaluating or implementing AI, automation, or other emerging technologies, including pilots and scale-up planning.
  • 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 communicate effectively with 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.
  • Ability to engage with global stakeholders across time zones as business needs require.

Responsibilities

  • Maintain the Regulatory Technology roadmap across Regulatory-owned platforms, aligning planned capabilities and investments with Regulatory priorities and the broader technology strategy.
  • Lead end-to-end demand intake and prioritization, 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 Digital Technology and Engineering teams, translating business needs into clear technology requirements and facilitating timely decisions, issue resolution, and cross-functional alignment.
  • Establish and facilitate roadmap and portfolio governance, providing visibility into 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 for releases and initiatives.
  • Communicate roadmap progress, delivery outcomes, risks, and recommendations to Regulatory leadership and cross-functional stakeholders.
  • Travel as required based on business needs.

About the Company

Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Vertex Pharmaceuticals develops medicines for serious diseases, with a focus on cystic fibrosis. It conducts extensive research and partners with other biotech firms to discover and develop new therapies, including ex vivo engineered cell treatments. Its products, such as ivacaftor, treat cystic fibrosis and other therapies undergo clinical testing to expand the pipeline. Revenue comes from selling approved drugs and from licensing and collaboration agreements. The company distinguishes itself through deep R&D investment, strategic partnerships, and a global reach aimed at addressing unmet medical needs. The overall goal is to bring effective new drugs to patients worldwide and improve outcomes and quality of life.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Boston, MA
Founded
1989

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