Medical Affairs Program Director

This role serves as the subject matter expert on Information Management Systems as it relates to IT, Telemedicine.  Serves as the medical leader on project teams responsible for generating technical solutions to ensure customer/business requirements and project deliverables are met.  Provides scientific expertise to support new Information Management technologies and product/process development (including design, development, analysis, troubleshooting).  Responsible for maintaining and continuously improving the quality system and achieving quality objectives through daily actions.
 
Key responsibilities include (but are not limited to):

• Serves as the subject matter expert on Information Management Systems as it relates to IT, Telemedicine, developing technologies
• Serve on project teams as GMA liaison and medical expert.  Provide guidance on customer needs (patient, HCP, payor) and promote medical differentiation of products.  Assess product risks and provide advice on risk mitigation.
• Collaborate with thought leaders on new diagnostic technologies: develops relationships with national thought leaders to stay current on latest experimental treatment modalities and their commercial opportunities, convent advisory boards for trial designs or to confirm appropriate product use of potential use of new products; maintain company brand visibility on a professional level; understand clinicians' needs and requirements and influence medical practice patterns; drive treatment protocol, adoption and appropriate reimbursement; ensure continued access to cutting edge industry trends and information.
• Medical and scientific expertise; input into product development, generate clinically robust and ethical outcomes studies; Directs pre-and-post marketing clinical trials.  Provides expert input into the design, execution and evaluation of trials that support the efficacy of medical devises; complete health hazard evaluations to determine potential patient impact; coordinate the use of outside medical opinions and ensure collaboration of internal medical and scientific resources.
• Global liaison: work with the clinical and medical groups within the global organization to identify and implement collaborative studies, regulatory activities and other programs.  Keep abreast of international research in related fields.
• Clinical spokesperson: Serve as clinical spokesperson in a wide range of venues, both internally and externally, such as professional society forums, customer sites, and relevant corporate functions.
• Work with Director Advice and Information Management to design, write, interpret data and publish clinical studies.
• Supervises contingent or intern staff
• May lead stand-alone projects or perform in collaboration with others