Key Responsibilities
Own end-to-end product strategy, vision, and multi-year roadmap for the MaxisAI platform.
Translate clinical trial, regulatory, and life sciences domain challenges into well-defined product opportunities.
Develop and maintain a prioritized product backlog aligned to customer value and business outcomes.
Lead product discovery, including customer interviews, competitive analysis, and market research.
Define and communicate product requirements through detailed PRDs, user stories, and acceptance criteria.
Partner with AI Engineering and Platform Engineering to guide architecture decisions and feature delivery.
Drive product positioning, feature differentiation, and go-to-market strategy in collaboration with Sales and Marketing.
Establish and track product KPIs including adoption, engagement, NPS, and revenue attribution.
Ensure product compliance with relevant GxP, HIPAA, and 21 CFR Part 11 regulatory requirements.
Champion a customer-centric product culture through continuous feedback loops and usability practices.
Engage directly with pharma, biotech, and CRO enterprise customers to shape product direction.
Manage the product lifecycle from ideation through release, iteration, and deprecation.

KPIs & Success Metrics KPI Target





Feature Release Cadence

Quarterly major releases

Customer NPS

>60

Product-led Revenue Attribution

>30% of ARR

Backlog Clarity (Story Readiness)

>85% sprint-ready

Regulatory Compliance Coverage

100% for GxP features

On-Time Feature Delivery

>85%

Required Experience
10+ years in product management, with at least 3 years in a senior/lead product role.
Domain experience in clinical trials, life sciences, health IT, or regulated SaaS environments strongly preferred.
Demonstrated track record of owning and shipping B2B enterprise software products.
Solid command of Agile product practices: backlog management, sprint planning, roadmap communication.
Experience working in or alongside AI/ML engineering teams.
Excellent written and verbal communication skills for executive, technical, and customer audiences.
Preferred Background
Understanding of clinical data standards (CDISC, USDM, ICH M11).
Exposure to GxP validation, 21 CFR Part 11, or regulated software settings.
Experience with AI-powered products or agentic workflows.
Prior experience at a healthtech, clinical tech, or pharma SaaS company

📌 Product Owner/leader Hyderabad
🏢 Maxis Clinical Sciences
📍 Hyderabad