Associate Director, Clinical Portfolio Technology

About the role

The Associate Director, Clinical Portfolio Technology at Alnylam is responsible for shaping, delivering, and continuously improving technology capabilities that support Clinical Delivery, Portfolio Management, and related Development functions.

Responsibilities

• Partner with Clinical Portfolio Services, Global Trial Optimization, Study Management, Data Science, Statistics and Epidemiology DSSE, and IT to translate business priorities into compliant, scalable, and user-focused solutions.
• Drive the successful delivery, adoption, and continuous improvement of technology capabilities that support clinical trial execution, study oversight, and portfolio decision-making across Development.
• Support the delivery, enhancement, and lifecycle management of platforms and capabilities that enable trial execution, study oversight, portfolio analytics, and data-driven decision-making across Development.
• Serve as a key liaison between Clinical Development and IT, ensuring business needs, technical considerations, risks, priorities, and trade-offs are clearly understood and effectively translated across teams.
• Coordinate with product owners, vendors, and internal IT teams to manage requirements, scope, dependencies, testing, issue resolution, and release readiness across clinical technology initiatives.
• Help ensure solutions are compliant, validated, and inspection-ready, consistent with GxP expectations, including 21 CFR Part 11, EU Annex 11, change control, documentation, and quality practices.
• Drive operational excellence and continuous improvement by identifying opportunities to simplify processes, improve data flows, reduce manual effort, and enhance the user experience across clinical systems.
• Apply broad knowledge of clinical trial technology, including the systems, integrations, data, and operational processes that support modern clinical delivery in a regulated environment.
• Collaborate with Quality, Security, Architecture, Infrastructure, Integration, Analytics, and application teams to ensure solutions are secure, scalable, supportable, and aligned with enterprise standards.
• Demonstrate strong learning agility and curiosity, with the ability to build knowledge in new domains and emerging capabilities, including AI, and apply them responsibly in support of Clinical Development.
• Contribute to a team culture defined by transparency, responsiveness, shared ownership, curiosity, and strong cross-functional partnership.

Qualifications

• Required: Bachelor’s degree in Information Technology, Computer Science, Life Sciences, or a related field; advanced degree preferred.
• 8+ years of experience in life sciences technology, including significant experience supporting clinical development platforms in regulated environments.
• Strong understanding of clinical trial processes, systems, and operating models, with the ability to translate operational needs into effective technology solutions.
• Working knowledge of GxP expectations, including 21 CFR Part 11, EU Annex 11, validation, change control, and inspection readiness principles.
• Experience working with major life sciences technology vendors and cross-functional delivery teams in support of regulated business processes.
• Strong communication and stakeholder management skills, including the ability to engage effectively with both business stakeholders and technical teams.
• Demonstrated collaboration, sound judgment, learning agility, and a hands-on approach to delivery and problem-solving.

Pay

$172,200.00 - $233,000.00