Clinical Researcher

Position Overview:

Lead the delivery of AI-driven clinical projects and validation studies ensuring transferable pipeline impact through product development and patient stratification models. Design and oversee clinical validation studies to generate evidence for the efficacy and safety of our AI solutions while managing research funding and external partnerships.

Key Responsibilities:

• Lead the successful delivery of multiple pharma, academic and internal AI-driven projects focused on healthcare, including scope management, detailed planning and strategic alignment with organization objectives
• Design robust clinical validation protocols in collaboration with NHS partners
• Manage end-to-end delivery of real-world evidence (RWE) research programs and implementation of digital tools in NHS cancer clinics
• Lead the creation and execution of a research dissemination strategy, leveraging findings to expand business opportunities and support strategic growth
• Serve as scientific lead for grant proposals and research funding calls to support internal research and evidence generation
• Manage the end-to-end delivery of clinical evaluations and validation of medical devices, including initiation of a multisite real world RCT within the NHS
• Be key point of contact for external engagements with academic experts, life science partners and research collaborators to enhance business development and drive new research opportunities
• Coordinate data collection and analysis for validation studies
• Ensure studies comply with ethical requirements and have appropriate approvals
• Analyze results and prepare reports for regulatory submissions
• Support publication of findings in peer-reviewed journals
• Develop case studies and evidence summaries for commercial presentations
• Collaborate with the legal team to ensure clear distinction of ownership of IP generated from projects
• Work with regulatory team to ensure product development plans align with medical device certification
• Engage regulatory advisors to assess medical device statuses according to FDA, MDR and UKCA requirements
• Lead on horizon scanning to understand market opportunity and assess feasibility of product rollout within NHS pathways

Requirements:

• Clinical background (MD, RN) or MSc/PhD in Clinical Research or related field
• 3+ years' experience managing clinical studies, preferably in digital health
• Knowledge of research methodologies applicable to AI validation in healthcare
• Understanding of NHS research governance frameworks
• Experience with HRA approval processes and Research Ethics Committees
• Strong project management and stakeholder engagement skills
• Excellence in scientific writing and presentation
• Experience with real-world evidence generation and medical device clinical evaluations
• Proven track record in securing research funding through successful bid submissions and grant applications
• Knowledge of regulatory requirements for medical devices (FDA, MDR, UKCA)
• Experience managing multi-site clinical trials within the NHS
• Demonstrated ability to lead cross-functional teams and manage complex stakeholder relationships