Qureight

Associate

• Support relationships with major pharmaceutical companies from initial research and engagement through partnership design and internal approval.
• Assess the scientific, clinical and commercial rationale for potential partnerships, therapeutic areas and technology-development opportunities.
• Analyse biomarker landscapes, including imaging, digital, molecular and clinical biomarkers.
• Monitor scientific, clinical, regulatory and market developments relevant to Qureight’s strategy.
• Evaluate new scientific capabilities, products and applications for Qureight’s technology and data.
• Prepare presentations, briefing papers, business cases and recommendations for the CEO, leadership team, Board and external partners.
• Support preparation for pharmaceutical, investor and strategic-partner meetings.
• Coordinate scientific, clinical, regulatory, product and commercial team input for strategic projects and partnership opportunities.
• Support commercial and scientific due diligence for partnerships, investments and other corporate-development opportunities.
• Help develop partnership structures, workplans, budgets and supporting documentation.
• Maintain records of strategic opportunities, decisions, actions and external engagements.
• Ensure agreed actions and priorities progress after internal and external meetings.
• Work closely with the CEO, CCO, CFO and multidisciplinary teams.

Corporate Development Associate

Product Manager

• Run the Platform team's day-to-day agile process, including sprint planning, backlog refinement, and prioritisation within the sprint
• Turn requirements and priorities set by the Head of Product Management into a well-organised, appropriately-sized backlog
• Translate user requirements and priorities into clear technical and architectural decisions
• Break requirements into implementation-ready user stories and technical tasks, working directly with engineers on approach and sequencing
• Define acceptance criteria and test specifications for backlog items
• Validate delivered work against acceptance criteria and test specifications before it reaches users
• Work embedded within the Platform team through planning, refinement, and review ceremonies
• Provide UX-informed input to feature design and prioritisation for external user products and Clinical Operations admin tooling
• Act as the Platform team's main point of contact for the Head of Product Management
• Surface technical constraints, feasibility, and delivery risks to inform prioritisation and roadmap decisions
• Ensure requirements and backlog items affecting GxP-relevant systems are documented and validated in line with Qureight's ISMS and Management of Software Policy

Product Owner

Clinical Research

• Deliver compliant clinical data and image management activities for commercial clinical study projects
• Perform image (DICOM file) quality control activities, including de-identification and visual screening, in line with work instructions and best practice
• Raise data queries and support external and internal staff in their resolution
• Conduct data reconciliation activities and deliver image and data transfer packages to sponsors and archival
• Support project/study managers in developing and agreeing data and image transfer specifications with sponsors, providing technical input where required
• Conduct user acceptance testing on project-specific configurations of the Qureight Imaging Platform
• Suggest and deliver revisions to work instructions and SOPs as part of continuous improvement
• Work with data engineers to develop improved methods and tools for managing clinical and image data
• Deliver activities on time and to a high standard
• Conduct work in line with Qureight SOPs, Good Clinical Practice guidelines, ISO27001 standards, and data privacy regulations
• Build strong relationships with sponsors, customers, and internal stakeholders through transparent and consistent communication

Clinical Data Manager

• Lead assigned customer projects and clinical studies from kick-off through maintenance and close-out
• Develop and maintain study plans, timelines, trackers and study management documentation
• Monitor study progress against milestones and identify risks, issues and dependencies
• Coordinate and lead study meetings, prepare agendas and status updates, and track actions
• Work with customers to establish project goals, objectives, requirements and expectations
• Collaborate and communicate with internal and external stakeholders
• Support clinical site managers and clinical data managers in delivering study milestones
• Deliver study start-up activities, including leading kick-off meetings and creating, reviewing and releasing key study documents
• Own and manage project-level change and risk management
• Monitor project financial milestones and work with Finance on invoicing timelines and deliverable tracking
• Deliver study management activities in accordance with Qureight SOPs, GCP guidelines, ISO27001 standards, data privacy regulations and applicable regulations
• Support Clinical Operations process improvement
• Report project financial details and milestone achievement to support invoicing and reconciliation

Clinical Study Manager

• Lead operational delivery of assigned customer projects and clinical studies from initiation through close out
• Ensure delivery against agreed scope and timelines
• Serve as subject matter expert for assigned studies
• Maintain oversight of study requirements, deliverables and operational performance
• Develop and maintain study plans, timelines, trackers and study management documentation
• Support clinical site managers and clinical data managers in delivering study milestones
• Collaborate with internal and external stakeholders
• Act as senior point of contact and trusted partner for assigned clients
• Establish and maintain long-term client relationships
• Lead client meetings, prepare agendas and status updates, and track actions
• Oversee study risks, issues and dependencies
• Develop mitigation and contingency strategies
• Deliver study start-up activities, including Kick-off Meetings and preparation, review and release of key study documents
• Manage project-level change and assess impacts on scope, timeline, resources and financial performance
• Oversee study financial milestones and contribute to forecasting, invoicing, reconciliation and deliverable tracking
• Deliver activities according to Qureight SOPs, GCP guidelines, ISO27001 standards, data privacy regulations and other applicable regulations
• Develop and maintain study management processes and write or review SOPs
• Support and mentor junior team members

Corporate Development Associate

Product Owner

Clinical Data Manager

Clinical Study Manager

Senior Clinical Study Manager