Medical Science Liaison - UK

DeepHealth, a RadNet company, is focused on delivering AI-powered solutions that improve population health, optimize radiology workflows, and drive earlier detection of disease. Our portfolio spans breast, lung, brain, prostate, and thyroid imaging AI, deployed across enterprise imaging platforms and large screening programs. 

The Medical Science Liaison will be accountable for the design, execution, and analysis of clinical studies that support the development and commercialization of innovative healthcare technologies. You will contribute clinical expertise as you collaborate with cross-functional teams, including R&D, regulatory affairs, legal counsel, product management, customer success, clinical development and medical affairs. It will be your responsibility to ensure scientific rigor, data quality, compliance with global regulatory standards, and relevance of the project objectives and outcomes to organizational goals.

• Clinical Research and Clinical Utility Expertise: Operate internally and externally as a subject matter expert in clinical imaging and technical workflow relevant to the specialty and modality of study — identifying barriers to success and owning proactive initiatives to improve the research progress.

• Clinical Evidence Strategy: Develop, deliver, and disseminate strategies to support the generation of compelling clinical evidence, as well as provide feedback and input on the product roadmap to product management, informing leadership decisions toward long-term clinical strategies.

• Partnership Development: Establish, manage, and steer partnerships with healthcare providers and affiliated research institutions and hospitals. Promote branding, messaging, and product innovations to strengthen and maintain these strong relationships.

• Research Program Initiation: Collaborate with internal teams and external partners to conceptualize, evaluate feasibility, plan, initiate, and support successful research programs.

• Manage and execute clinical studies including creating project plans, RACI charts, communication strategy, budget proposals, timelines, defining project deliverables, and contractual agreements, as well as developing essential documents such as study protocols, IRB submissions, subject materials, recruitment processes, data management and data analysis plans, and coordinating the engagement of multiple stakeholders.

• Ensuring adherence to Good Clinical Practice (GCP), ethical standards, and applicable regulations to protect the validity and integrity of the company’s sponsored collaborations.

• Collaborate professionally with cross-functional teams, including data scientists, engineers, physicians, and researchers to integrate clinical insights into product design and refinement.

• Work on-site with healthcare professionals and clinical collaborators to gather clinical feedback, identify unmet needs, and validate clinical use cases in Beta phase as well as support the evaluation, implementation, troubleshooting, and optimization of research products in real-world environments.

• Serve as the primary point of contact for innovation partner sites, facilitating effective communication and coordination of multi-disciplinary research initiatives.

• Provide clinical expertise in interactions with regulatory authorities and external partners.

• Develop scientific presentations and publications to support Marketing activities and spotlight the credible clinical evidence that reinforces product claims and proof points.

• Ensure the company’s offerings are accurately and consistently represented to healthcare providers.

• Analyze and interpret clinical data to evaluate the safety, efficacy, and performance of products.

• Nurture KOL relationships and grow the Advisory community.

PLEASE NOTE: This is not an exhaustive list of all duties, responsibilities and requirements of the position described above.  Other functions may be assigned and management retains the right to add or change duties at any time.