Job Description

The Manager, Medical Affairs will provide expertise as well as clinical development and technical knowledge to the Intelligent Diagnostics (IntDiag) category. Products in the IntDiag category enable earlier diagnosis through improved access and digital examination tools for accurate physical assessment. Critical to this role is global and regional clinical knowledge of medical devices, environments of care and data use as well as the ability to offer mentorship for product development support. The Manager, Medical Affairs is accountable for establishing, nurturing, and maintaining strong collaborative relationships with critical WWM colleagues (such as Clinical Research, HEOR/RWE, Global Patient Safety, and WWM Strategy and Delivery) as well as cross-function partners (such as R&D, Marketing, Quality) to enable a highly efficient and effective working environment. Responsibilities include serving as the medical and device subject matter expert to both internal and external customers for product development, risk assessment, training, implementation, literature reviews, and complaints; providing accurate, balanced and timely clinical expertise to functional areas such as clinical development, R&D, marketing, manufacturing, quality assurance, regulatory affairs, and legal based on objective evidence and clinical experience; providing clinical expertise for creation and development of risk assessments and quality standards for product design history files; devising novel approaches to address clinical and technical problems in clinical practice through development and modification of related medical devices; assimilating voice of customer and clinical experience for design input with new product development and product lifecycle management; developing and delivering relevant medical device training programs that support product implementation, training, and marketing efforts; training internal customers on product application, disease states, and regional differences as required; supporting product implementation process creation, maintenance, and controlled launch when applicable; maintaining familiarity of published literature as objective evidence for clinical trends and therapies related to impact on product lines; and coordinating with other Medical Partners as needed to support Division Medical efforts. Requirements include minimum 5 years of related clinical experience; degree in related clinical field (advanced degree preferred) or proven experience; NP/PA/MD with primary and/or acute care experience such as ER, Urgent Care, or Hospitalist/internal medicine is ideal; optometrist with sophisticated knowledge of physical assessment considered; medical affairs proven experience highly preferred; active license in a U.S. state or territory in standing required with clinical expertise; excellent written, verbal communication, and organizational skills; effective and proficient presentation and teaching skills; self-motivated, multi-tasking, with outstanding follow through; ability to travel frequently (up to 50%) domestically and occasionally internationally. Applicants must be authorized to work for any employer in the U.S. Baxter is unable to sponsor or take over sponsorship of an employment visa at this time.

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