Qureight is a healthcare and biotechnology company applying artificial intelligence to precision medicine and drug development. Its platform curates and analyzes complex healthcare data, combining medical imaging, clinical information, physiological measurements, and biomarkers into structured, usable datasets. Qureight works with biopharmaceutical companies, contract research organizations, hospitals, and healthcare institutions, with a focus on lung and heart diseases. Its AI-enabled workflows and image-analysis tools support research in areas including interstitial lung disease, pulmonary hypertension, and lung cancer, helping teams identify insights from clinical-trial and real-world data. The company’s work spans collaborative data analysis, machine learning, and technology designed to support more informed decisions throughout the drug-development process.
Clinical Study Manager - Qureight (Cambridge Hybrid)
Manage clinical study start-up, delivery and close-out for Qureight’s AI-powered imaging platform. Coordinate milestones, risks, stakeholders and compliant trial execution.
Description
- Manage assigned customer projects and clinical studies from initiation through maintenance and close-out
- Create and maintain study plans, schedules, trackers and management records
- Track milestone progress while identifying risks, issues and dependencies
- Organize study meetings, prepare agendas and updates, and follow up on actions
- Partner with customers to define project objectives, requirements and expectations
- Maintain effective communication with internal and external stakeholders
- Help clinical site and data managers achieve study milestones
- Lead start-up work, including kick-off meetings and the preparation, review and release of essential study documents
- Manage project-level changes and risks
- Track financial milestones, invoicing schedules and deliverables with Finance
- Conduct study management in line with Qureight SOPs, GCP, ISO 27001, privacy requirements and applicable regulations
- Contribute to Clinical Operations process improvement
- Report financial progress and milestone completion to support invoicing and reconciliation
Requirements
- At least two years of clinical research experience, preferably in an imaging CRO or clinical trial delivery setting
- Project management or clinical research start-up experience is preferred, especially with pharmaceutical lung and heart trials
- Clinical trial imaging experience is highly preferred but not required
- Demonstrated ability to build and sustain relationships with internal and external stakeholders
- Working knowledge of ICH Good Clinical Practice (GCP), supported by recent training
- Experience operating within a Quality Management System such as ISO 9001 or ISO 13485
- Familiarity with applicable regulatory, compliance and industry standards, including 21 CFR Part 11
- Excellent interpersonal skills with strong written and verbal communication
- Proven ability to work effectively and solve problems in a technical, innovative environment with close attention to detail
- Persistent, proactive approach to achieving objectives
- Project management experience or a formal project management qualification
- Relevant scientific or technical degree is advantageous but not required
- Applicants must submit a CV and covering letter
- Understanding of clinical study quality and regulatory requirements
- Ability to work from the Cambridge or London office in a hybrid setup
Benefits
- Annual bonus opportunity
- Private medical cover
- Life insurance
- Cycle-to-work benefit
- Employer-contributory pension
- Equity participation
- 28-day holiday allowance
- 25 days of annual leave
- Three additional company days between Christmas and New Year
- Bank holidays
- Enhanced family leave
- Collaborative workplace with multidisciplinary specialists