Group Product Manager – Clinical and Data Monitoring Technologies in London

At CluePoints, we're redefining how clinical trials are run. As the premier provider of Risk-Based Quality Management (RBQM) and Data Quality Oversight software, we harness advanced statistics, artificial intelligence, and machine learning to ensure the quality, accuracy, and integrity of clinical trial data, helping life sciences organizations bring safer, more effective treatments to patients faster. We're proud to be an ambitious, fast‐growing technology scale‐up with a dynamic and diverse international team representing more than 20 nationalities. Collaboration, flexibility, and continuous learning are part of our DNA. At CluePoints, you'll find a culture where you can grow, make an impact, and have fun along the way. Guided by our values of Care, Passion, and Smart Disruption, we're united by a shared mission: to create smarter ways to run efficient clinical trials and deliver AI‐powered insights that improve human outcomes worldwide.

We're looking for a Group Product Manager – Clinical Data & Monitoring Technologies to join our Product Management group and contribute to our mission of transforming clinical research through data‐driven insights. This individual will bridge clinical data operations with product management, leveraging insights from their own experience as a data manager/central monitor to build products that improve data quality, risk‐based monitoring and trial efficiency. The GPM will serve as a player–coach—overseeing product strategy while mentoring and managing a team of product managers.

Job Requirements

• Clinical data management / central monitoring experience (4–6 years).
• Hands‐on experience designing data management plans and managing data cleaning and query resolution processes.
• Experience in centralized monitoring roles such as subject‐level data review, KRI trending and risk‐based monitoring strategies.
• Familiarity with regulatory frameworks (ICH GCP), clinical trial protocols, risk‐based quality management and industry data standards (e.g., CDISC).
• Proven experience analyzing complex clinical and operational data, identifying patterns and risks, and communicating findings to study teams.
• Product management experience (2–4 years).
• Experience owning the product lifecycle—from ideation and requirements gathering to release and iteration.
• Able to create product roadmaps, business cases and go‐to‐market strategies.
• Demonstrated success working with cross‐functional teams (engineering, design, marketing, sales) to deliver products in a regulated or clinical technology environment.
• Familiarity with agile methodologies, backlog management and iterative development.
• People management experience leading and mentoring product managers or cross‐functional teams.
• Ability to set clear goals, provide constructive feedback and drive accountability.

Skills And Qualifications

• Bachelor's or advanced degree in life sciences, statistics, computer science, public health or a related discipline.
• Deep understanding of clinical trial processes and data flows, including central monitoring, data management, biostatistics and clinical operations.
• Strong analytical and problem‐solving skills; ability to interpret complex datasets, identify risks and propose data‐driven solutions.
• Proficiency with clinical data systems (e.g., EDC, CTMS), analytics tools and business intelligence platforms; working knowledge of SQL, SAS or R is advantageous.
• Excellent communication skills (verbal, written and presentation). Able to tailor messages to technical and nontechnical audiences and facilitate stakeholder alignment.
• Demonstrated leadership and people management skills—coaching, performance management, conflict resolution and team motivation.
• Ability to manage multiple projects and competing priorities in a fast‐paced environment.
• Cultural awareness and ability to work effectively with global teams.
• Technically savvy with keen interest and experience on AI tools.

Job Responsibilities

• Strategy and product leadership: Define product vision and roadmap: develop a cohesive product strategy that aligns with business goals and customer needs. Communicate the roadmap to senior leadership and stakeholders, set measurable goals and monitor progress.
• Stakeholder engagement: Build relationships with internal and external stakeholders, including clinical data managers, central monitors, statisticians, investigators, IT and commercial teams. Gather feedback, manage expectations and ensure products meet regulatory and operational needs.
• Mentorship and team management: Lead, coach and inspire a team of product managers. Provide regular feedback, set clear objectives and foster a culture of accountability and continuous learning. Act as a "player/coach"—balancing hands‐on product work with people management responsibilities.
• Product development & execution: Translate domain expertise into product design: use your understanding of clinical data management and centralized monitoring to oversee the design of solutions that streamline data capture, cleaning and risk‐based oversight.
• Ensure data quality and compliance: incorporate regulatory requirements (e.g., ICH, GCP, CDISC standards) into product features. Design tools that support risk‐based monitoring strategies, patient safety and early detection of data quality issues.
• Conduct user research and validation: work closely with clinical data managers, monitors and study teams to gather requirements, test prototypes and iterate products. Facilitate workshops to refine features and workflows.
• Analyze product performance: establish key performance indicators (KPIs) to enable analytics to track adoption and test hypothesis. Use findings to prioritize enhancements and influence strategic decisions.
• Cross‐functional collaboration: Partner with engineering and design: provide domain context and clarify acceptance criteria and use cases. Communicate across the organization: report progress, risks and product value to executive leadership and cross‐functional partners. Represent the voice of the customer and advocate for user‐centered solutions.

Job Benefits

• Private Medical Insurance through Vitality Health (full hospital cover, 24/7 GP, and therapy sessions)
• Group Critical Illness Cover with Aviva Life Insurance (death‐in‐service lump sum)
• Pension Scheme with 9% employer contribution via Scottish Widows
• Opportunities for professional development and sponsored certifications
• A hub‐based hybrid model that blends flexibility with purpose—connecting teams through collaboration, learning, and a vibrant social culture.

Why join us?

This role offers an opportunity to shape the next generation of clinical data and monitoring technology. You will leverage your data management expertise to build products that improve patient safety and trial efficiency while leading a team of motivated product managers. Join us to help transform how clinical trials are conducted and bring innovative therapies to patients faster.

Equal Opportunities & Data Protection Statement

CluePoints is an equal opportunities employer. We celebrate diversity and are committed to creating an inclusive environment for all employees and applicants. We welcome applications from all individuals regardless of age, disability, gender identity or expression, marital or civil partnership status, pregnancy or maternity, race, religion or belief, sex, or sexual orientation. Any personal data you share during your application will be processed in accordance with the UK GDPR and the Data Protection Act 2018 and will be used solely for recruitment purposes. By submitting your application, you consent to the processing of your data for recruitment and employment purposes. At CluePoints, we believe that diverse teams make better decisions and drive innovation. We're committed to building a workplace that reflects the communities we serve and where everyone can thrive.