This post is also available in: Svenska (Swedish)

Assignment Description:

We are looking for a Senior eConsent Product Owner to join our dynamic team.

What you will work on:

• Lead the development of GxP-compliant software solutions supporting clinical trials within the eConsent product area
• Define and communicate the product vision, strategy, and roadmap, ensuring alignment with business goals, regulatory standards, and technical feasibility
• Collaborate with Product Managers, engineers, UX designers, architects, regulatory experts, and clinical stakeholders to deliver impactful, compliant solutions
• Own and manage the product backlog in JIRA, ensuring features and requirements support PI objectives and meet GxP and 21 CFR Part 11 compliance
• Drive the product lifecycle from discovery to delivery, transforming business needs into actionable development requirements and sprint goals
• Document requirements, workflows, acceptance criteria, and maintain traceability, compliance, and risk documentation
• Prioritize features, bug fixes, and technical debt while balancing near-term delivery with long-term strategic vision
• Facilitate agile ceremonies, lead backlog refinement, and drive a culture of continuous improvement, collaboration, and accountability
• Coordinate and align cross-functional feature teams, managing interdependencies between front-end, app, and platform components
• Support estimation, planning, and early-stage analysis of upcoming initiatives to ensure smooth execution and delivery readiness

What you bring:

• 10+ years of project management and delivery experience with a strong technical foundation
• Proven track record in delivering large, complex technical solutions in international and regulated environments
• Strong understanding of software architecture, particularly for front-end and integrated system solutions
• Demonstrated experience in leading and motivating cross-functional teams toward successful delivery outcomes
• Hands-on experience with validation of computerized systems within GxP or other regulated frameworks
• Technical fluency with clinical research systems and the ability to translate complex requirements into clear development items
• Proficiency in tools such as JIRA, Confluence, and regulatory documentation platforms
• Solid understanding of Agile methodologies and practical experience driving Agile product delivery
• Background in clinical trials, pharma, life sciences, or health tech industries is highly desirable

If this sounds interesting, please send your CV to cv@veritaz.se