Mgr Medical Affairs - Clinical Scientist

Mgr Medical Affairs - Clinical Scientist - req1715 Overview Work as part of a dynamic and fast-paced team of clinical and technical experts dedicated to positively impacting clinical care by effectively translating innovative imaging solutions to the clinical environment. Generate scientific and clinical evidence via product evaluations and research in order to highlight advantages of the technology while maintaining alignment with the business strategy. Participate as a technical expert of the product line technology and communicate product intelligence to internal teams, key partners, collaborators, and external experts. Effectively interact with multiple teams including R&D, global and local business, marketing solutions, regulatory, applications, and service. Manage key clinical customer/partner relationships in order to comprehensively support Canon's business objectives while serving the needs of patients. Responsibilities This is a remote based position in the USA KOL and strategic partner engagement Develop and implement strategy to identify, engage, and sustain relationships with KOLs and strategic partners across clinical specialties for modality. Ensure KOL and partner engagement activities align with corporate and modality strategies, product development / technology roadmaps, and regional market needs. Maintain standardized and compliant engagement frameworks, governance models, and reporting mechanisms. Coordinate communications between KOLs, strategic partners, modality team(s) and other Canon stakeholders. Clinical research and validation Manage collaborative research and clinical evaluation projects at collaboration/partner sites including data collection, protocol development, data acquisition, phantom studies, equipment evaluations, post processing, co‑writing papers, IP and technology transfer support, and development of presentations. Provide evidence-based guidance on scientific and clinical requirements for new products and features to meet market needs. Support regulatory activities providing technical/market expertise, and reviewing study/test‑plan design. Influence regulatory specifications and claims strategy by providing scientific and clinical consultation during early phase development. Support, design, and execute internal and external product evaluations. Explore expansion of clinical use. Provide product validation results and communicate scientific and clinical benefits to company stakeholders including modality business unit (BU) teams, marketing, and applications for the purposes of product collateral development and education. Capitalize activities through the development of marketing collateral by leveraging relevant scientific and clinical data, ensuring scientific accuracy through thorough review, and collaborating with regulatory to maintain compliance with clinical claims and technical specifications. Cross‑functional collaboration Work with modality BU team(s) to evaluate product claims and specifications, including testing of default protocols to ensure acceptance by industry standards (e.g., The Joint Commission and ACR). Communicate relevant evaluation results via appropriate channels to internal and global research teams. Contribute to the development of scientific and clinical value propositions for modality products, as well as competitive differentiation and counter‑arguments. Support education teams in development of videos and training programs by providing clinical and technical expertise and evidence. Support Medical Advisory Board (MAB), User Group, or similar forums related to the product line. Work with database administrator(s) to ensure research activities are kept to schedule, remain compliant, and updates are recorded on a regular basis. Participate in modality BU and Medical Affairs meetings and provide clinical and technical expertise to support business decisions. Provide clinical, technical, and product education to enhance the knowledge base of the Commercial, Marketing, Applications, and Service teams. Collaborate with healthcare economics personnel to translate economic benefits of clinical research programs for the benefit of marketing and sales programs. Communicate known clinical or technical product issues via appropriate channels. Work with relevant team(s) (e.g., Strategic Development, Regulatory, and Service) to quickly implement market‑accepted solutions. Perform all responsibilities in full compliance with regulatory and legal requirements, and within industry guidelines such as the AdvaMed Code of Ethics. Represent Canon as a spokesperson for product line technology at educational and scientific industry events. Represent Canon in industry organizational activities (e.g., AdvaMed, MITA, IEC, AAPM, RSNA, ISMRM, ACR, ABR, QIBA, etc.). Other duties as assigned. Pay Range $112k-$203K DOE Qualifications PhD, MD, or equivalent in medical imaging physics, engineering, or one of the clinical sciences. 5 years of experience working with the product line technology as a Medical Physicist, Scientist, or MD in a clinical physics or clinical research setting. Strong communication skills, including credible interaction with prominent academics and physicians and demonstrated skill at scientific writing and presenting. Demonstrated project management and/or customer support skills. Demonstrated understanding of current and emerging products and technology in modality product line. Detailed clinical and technical knowledge of product line technologies (CT, Healthcare IT, MI, MR, XR, Ultrasound and/or Interventional systems). Proficiency with computers in windows‑based software environment. Proven ability to operate effectively in a matrix organizational structure. Must be capable of lifting up to 25 pounds. All qualified applicants will receive consideration for employment without regard to race, sex, color, sexual orientation, gender identity, religion, national origin, protected veteran status, or on the basis of disability. #J-18808-Ljbffr