![]() Training in a surgical discipline is required. An MD/DO from an accredited school is required for this position. ![]() ![]() Write key scientific and clinical publications highlighting critical findings in the field and cementing role as KOL in the field. Attend key Scientific Meetings, participating as an oral presenter.copy review, medical information requests, medical input into clinical evaluation reports, etc.). Provide lifecycle medical affairs support (e.g.Provide critical evaluation of current literature and competitive activity, and in other domains where medical and scientific expertise is required.Participate as an active member of the Platform Leadership Team, representing the Medical, Clinical and Pre-Clinical functions. Provide support to commercial teams by providing medical and scientific expertise to drive optimal business strategic direction and tactical business activities, including product launches, key scientific meetings, relationship management with leading research physicians and medical delivery system or government decision makers.Provide scientific and medical perspectives for management of requests for Educational Grants, requests for Scientific Information, and requests for Investigator Initiated Research Grants.Provide support to New Business Development.Internally focused activities consist of pipeline engagement, clinical strategy, safety/surveillance and compliance, while externally facing activities aim to drive deeper and broader customer engagement and insight generation. Participates as part of the Clinical, Medical and Pre-Clinical Evidence Team to achieve the strategic goals and activities of the function(s).Drive the creation of ‘Target Product Profile’ documents that spell out the value proposition and potential claims of the desirable new product. Participate within the new product development R&D teams, by providing expert medical and scientific input, including conceptual and hands-on product evaluation, and clinical research perspectives.Participate or lead clinical scientific discussions with regulatory agencies / notified bodies to drive support of the clinical and regulatory strategy, including proposed clinical investigations review process of clinical evidence generated for marketing authorization, line extensions, etc., including during sponsor regulatory inspections. ![]() Contribute to medical input into risk management plans and failure mode analysis during product development and safety signal detection and post-market surveillance post-launch.
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