Your day to day
- Translate Strategy into Execution
- Partner with product managers and stakeholders to break down high-level product strategies into clear, detailed epics and user stories
- Serve as the voice of the customer in agile ceremonies, ensuring the team is always aligned on delivering business and user value
- Support creation of wireframes and prototypes to visualize workflows and improve user experience
- Collaborate with engineering and UX teams to refine requirements, review prototypes, and validate deliverables throughout the sprint cycle
Facilitate Agile Collaboration
- Participate in all agile rituals, including sprint planning, backlog grooming, reviews, and daily standups
- Maintain a well-prioritized product backlog, ensuring clarity, consistency, and alignment with roadmap goals
- Collaborate cross-functionally with QA, documentation, services, and support teams to ensure successful product releases
Contribute to Market & Domain Intelligence
- Research and document industry trends, competitive offerings, and evolving customer needs
- Stay informed on clinical trial standards, data workflows, and regulatory requirements
- Contribute to knowledge sharing across the organization through release notes, internal trainings, and support materials
Education & Experience
- Bachelors degree in a life sciences discipline, computer science, or related field, or equivalent work experience preferred
- 5+ years of experience in a product owner, business analyst, or clinical data role within life sciences technology or clinical trials preferred
- Hands-on experience with agile product development processes and tools (e.g., Jira, Confluence, ProductBoard)
- Prior experience working on a cloud-based SaaS platform strongly preferred
Professional Skills
- Strong understanding of product development lifecycle and user-centered design principles
- Proven ability to write clear, concise user stories and acceptance criteria
- Excellent communication and interpersonal skills; comfortable presenting ideas and facilitating cross-team discussions
- Highly organized with strong attention to detail and the ability to manage multiple priorities
- Curious, analytical mindset with a passion for solving real-world problems in clinical research
Technical & Domain Skills
- Familiarity with clinical trial workflows, EDC systems, and regulatory standards (e.g., CDISC, 21 CFR Part 11, IHC E6) is a plus
- Experience creating or reviewing clinical metadata and working with data visualization tools is desirable
- Working knowledge of agile methodologies and best practices for backlog management