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Product Manager, Clinical Development Platforms

BeiGene

Any City, USRemotePosted 4 days ago$155,000 - $200,000 annually
Full TimeSenior LevelProgram / Project ManagementBiotechnology
Original posting ↗

Summary

The Product Manager is responsible for product vision, strategy, roadmap planning, requirements, delivery support, adoption, and continuous improvement throughout the product lifecycle. The role works closely with business stakeholders, engineering, data, AI, UX, and quality teams to deliver digital solutions that improve efficiency, decision-making, compliance, and user experience across the clinical development lifecycle.

Job description

Core Product Management Responsibilities

  • Define and maintain product vision, strategy, roadmap, and success metrics.
  • Partner with business stakeholders to identify opportunities, pain points, and desired business outcomes.
  • Conduct discovery activities, including stakeholder interviews, workflow analysis, current-state and future-state assessments, and end-to-end understanding of users, personas, journeys, pain points, and desired outcomes.
  • Partner with UX/Design to translate discovery insights into detailed journey maps, service-experience designs, prototypes, and usability validation.
  • Develop product roadmaps based on business value, strategic priorities, risk, complexity, dependencies, and resource constraints.
  • Lead prioritization of product capabilities, features, enhancements, and enabling investments.
  • Create and maintain business cases and value hypotheses for product investments.
  • Assess market and technology trends, vendor solutions, and build-versus-buy opportunities.
  • Establish product success measures and track adoption, value realization, user satisfaction, and operational impact.
  • Translate business needs into clear product requirements, workflows, use cases, business rules, and acceptance criteria.
  • Ensure requirements are complete, testable, traceable, and ready for development.
  • Facilitate product decisions, prioritization, and scope tradeoffs across stakeholders.
  • Define product boundaries and identify business, workflow, system, integration, and data dependencies.
  • Apply systems thinking to understand how users, decisions, workflows, information, and products interact across the clinical-development ecosystem.
  • Collaborate with technical teams to evaluate solution options and make informed product decisions.
  • Participate in backlog refinement, release planning, roadmap reviews, and product governance checkpoints.
  • Ensure alignment between business objectives, approved scope, and delivered product capabilities.
  • Support products throughout discovery, workflow analysis, validation, design, development, release, adoption, support, and continuous improvement.
  • Own product vision, roadmap, prioritization, requirements quality, acceptance criteria, stakeholder alignment, release-scope definition, and measurable outcomes.
  • Partner with business stakeholders on adoption, change management, communications, training, and value realization.
  • Establish structured mechanisms for post-release feedback, support intake, backlog triage, and product learning.
  • Monitor product performance and identify opportunities to improve outcomes and user experience.
  • Facilitate release readiness with business, quality, delivery, and technical teams.
  • Maintain alignment and communicate product decisions throughout planning and delivery.
  • Establish clear product decision rights, including who recommends, contributes, approves, is informed, and serves as the escalation authority.
  • Identify and manage product risks, assumptions, business dependencies, and cross-product impacts.
  • Partner with Technical Leads and Architects on solution options, feasibility, non-functional requirements, technical dependencies, and risks.
  • Partner with Project, Program, or Delivery Management on integrated plans, schedules, RAID management, release coordination, and cross-team follow-through.
  • Influence cross-functional teams without formal authority and communicate effectively with business and executive stakeholders.
  • Produce fit-for-purpose product artifacts, including discovery summaries, stakeholder maps, workflows, use cases, PRDs, roadmaps, decision logs, dependency maps, release scope, and product metrics.
  • Identify opportunities to use AI, including generative and agentic AI, automation, analytics, and decision intelligence to improve user outcomes and productivity.
  • Define AI use cases, intended use, human-in-the-loop workflows, business requirements, user controls, evaluation criteria, measurable outcomes, and adoption needs for AI-enabled features.
  • Collaborate with Data Science, AI, Engineering, Architecture, Quality, and domain experts to deliver responsible and measurable AI capabilities.
  • Define expected outputs, validation approaches, quality criteria, representative test scenarios, and human review expectations.
  • Use AI-assisted methods to accelerate discovery synthesis, requirements critique, workflow analysis, prototyping, and identification of gaps.

Clinical Development Domain Responsibilities

  • Develop a strong understanding of clinical development, clinical operations, regulatory, safety, data management, medical writing, and related business processes relevant to the assigned product portfolio.
  • Partner with R&D stakeholders to understand clinical workflows, operating models, user needs, decision points, data needs, and compliance expectations.
  • Translate complex clinical, scientific, and operational processes into scalable digital-product capabilities.
  • Collaborate across functions to improve process efficiency, quality, compliance, traceability, and user experience across the clinical development lifecycle.
  • Support digital transformation initiatives that improve planning, execution, oversight, documentation, and decision-making.
  • Understand clinical information and logical data flows at a product level, including what information is needed, where it originates, who consumes it, the decisions it supports, and the upstream/downstream impact of change.
  • Apply appropriate product controls for regulated or validated solutions, including auditability, role-based access, data integrity, testing evidence, and controlled release expectations.

Preferred Domain Focus: Protocol Authoring and Workflow Automation

Experience in one or more of the following areas is highly desirable but is not required across every area:

  • Clinical protocol authoring or digital protocol solutions
  • Study design platforms and Schedule of Activities
  • Clinical document management or medical writing platforms
  • CRF design, clinical data collection, or study setup automation
  • Protocol amendments, version management, comparison, lineage, or change-impact assessment
  • Workflow automation, structured content, traceability, or metadata management
  • AI-assisted content authoring, document intelligence, extraction, or review
  • Clinical-trial technology ecosystems and interconnected downstream workflows

Requirements

  • Bachelor's degree in Computer Science, Health Sciences, Life Sciences, Engineering, Business, or a related field.
  • Five or more years of Product Management experience delivering enterprise software or digital products.
  • Experience partnering with business stakeholders to define product strategy, roadmaps, requirements, and measurable outcomes.
  • Strong discovery, end-to-end journey and workflow analysis, systems thinking, prioritization, facilitation, and problem-solving skills.
  • Experience translating user needs into product requirements, use cases, business rules, acceptance criteria, and delivery-ready work.
  • Excellent verbal, written, presentation, and stakeholder-management skills.
  • Proven ability to influence cross-functional teams without direct authority.
  • Experience working in Agile or iterative product-delivery environments.
  • Strong analytical judgment and the ability to balance strategic thinking with execution focus.
  • Experience in life sciences, healthcare, biotechnology, pharmaceuticals, clinical research, or another regulated environment.
  • Experience supporting Clinical Development, Clinical Operations, Regulatory, Safety, Medical Writing, Data Management, or related functions.
  • Experience delivering GxP, validated, or otherwise regulated digital products.
  • Experience defining or delivering AI-enabled, including generative or agentic AI, analytics-driven, decision-support, or workflow-automation products, with an understanding of human-in-the-loop workflows and measurable product outcomes.
  • Experience collaborating with UX/Design, Data, AI, Analytics, Architecture, Quality, and Engineering specialists on complex enterprise products, with clear understanding of cross-functional ownership boundaries.
  • Experience managing cross-product dependencies, integrations, traceability, versioning, or upstream-to-downstream workflows.
  • Experience with protocol authoring, study design, or Schedule of Activities solutions.
  • Familiarity with clinical-trial technology platforms and digital R&D ecosystems.
  • Experience with clinical document automation or intelligence solutions.
  • Knowledge of clinical data standards, structured protocol models, or metadata management.
  • Experience with AI-assisted authoring, decision support, content extraction, or document intelligence.
  • Familiarity with Veeva, Medidata, Oracle, IQVIA, or related clinical-technology ecosystems.
  • Advanced degree in a relevant business, technology, clinical, scientific, or health discipline.

Benefits

  • Medical, Dental & Vision
  • 401(k)
  • FSA/HSA
  • Life Insurance
  • Paid Time Off
  • Wellness
  • Annual bonus plan
  • Discretionary equity awards
  • Employee Stock Purchase Plan

Company overview

BeiGene, Ltd., now rebranding as BeOne Medicines, is a global commercial-stage biotechnology company specializing in the discovery, development, manufacturing, and commercialization of innovative oncology medicines. Founded in 2010 by John V. Oyler and Xiaodong Wang, the company has grown into a multinational organization with headquarters in Cambridge, Massachusetts, Beijing, China, and Basel, Switzerland. BeiGene focuses on developing targeted and immune-oncology therapies for cancer treatment, with a diverse pipeline that includes internally discovered products like BRUKINSA (zanubrutinib), a Bruton's tyrosine kinase inhibitor, and Tevimbra (tislelizumab), a PD-1 inhibitor. The company operates across six continents with over 45 countries participating in clinical trials and has enrolled more than 30,000 patients in its research programs. With approximately 12,000 employees worldwide, BeiGene has established itself as a significant player in global oncology, particularly with strong market presence in China and expanding operations in the United States and Europe. The company's mission centers on expanding access to high-quality cancer therapies worldwide through persistent innovation and challenging traditional approaches to drug development.

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