Group Product Manager
CluePoints
Group Product Manager
CluePoints
Cloud-based RBQM platform for clinical trials
Translate company strategy and Market Owner direction into actionable squad-level outcomes, owning the OKR cascade from domain strategy to squad goals.
Own roadmap prioritisation and portfolio-level trade-off decisions, and remain accountable for domain-level business outcomes.
Co-define the go-to-market approach for your domain with Market Owners, and hold the quality bar for enablement materials produced by your team.
Represent the domain at leadership level and act as the escalation point for major product or customer issues.
Set and maintain discovery standards across all squads in your domain; join discovery calls to challenge surface-level findings, deepen questions and surface edge cases and biases.
Ensure success metrics are defined and used consistently across your portfolio, reviewing portfolio-level metric health and surfacing business risk before it becomes visible to leadership.
Hold the team accountable to outcomes rather than velocity, coaching PMs away from output and feature-factory thinking.
Ensure no feature ships without appropriate regulatory and quality consideration, applying GxP-aware standards consistently across the portfolio.
AI-First Ways of Working & Cross-Functional Partnership
Coach PMs on AI-assisted ways of working, ensuring the team reviews and challenges AI-generated artefacts and does not revert to manual-first habits.
Maintain a cohesive vision, goals and processes with peer GPMs; proactively align to avoid fragmentation of the PM practice and surface cross-domain dependencies early.
Act as the voice of the customer in release planning, influencing release sequencing and validation priorities (advocating within release management and validation, not owning them).
Act as the primary interface with Sales, Customer Engagement and Professional Services for your domain, ensuring consistent, high-quality enablement at launch.
Ensure every PM on your team has sufficient direct customer access and remove blockers to continuous discovery.
•Proven product management experience at Product Manager level or above, with a track record of owning outcomes and metrics across discovery to delivery.
•Demonstrated people leadership: coaching, performance management and career development of Product Managers (or equivalent product practitioners).
•Experience translating strategy into squad-level outcomes, including OKR-based planning and portfolio-level prioritisation and trade-offs.
•Working knowledge of regulated software development (GxP and audit readiness) and the ability to apply regulatory and quality standards to product decisions.
•Credible stakeholder management with Market Owners, Strategy, Engineering, Sales and customer-facing teams, including senior leaders.
•Excellent communication skills, able to represent a domain at leadership level and to resolve messaging and positioning conflicts.
Experience recruiting and onboarding product talent, and building team standards that others reference.
Practical AI fluency: comfortable working AI-first and coaching a team to review and challenge AI-generated specifications and artefacts.
Cloud-based RBQM platform for clinical trials
CluePoints provides risk-based quality management and data quality oversight software for clinical trials. Its cloud-based platform analyzes trial data using advanced statistics, machine learning, and AI to identify risks and monitor data quality from initial risk assessment through issue tracking. Key products—Site Profile and Oversight Tool (SPOT), Intelligent Medical Coding (IMC), Intelligent Query Detection (IQD), and Medical & Safety Review (MSR)—automate data discrepancy detection, improve medical review efficiency, reduce manual coding, and enable adaptive site monitoring. The company differentiates itself with an end-to-end, multi-product platform (expanded in 2024) that combines RBQM, data analytics, and regulatory-aligned monitoring to help pharmaceutical/biotech companies and CROs de-risk trials and ensure data integrity and patient safety. Its goal is to help customers meet regulatory guidance from bodies like the FDA and EMA while improving trial quality and efficiency.
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