.This job is with Thermo Fisher Scientific, an inclusive employer and a member of my Gwork – the largest global platform for the LGBTQ+ business community.Please do not contact the recruiter directly.Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description PURPOSE OF THE FUNCTION The Medical Science Liaison (MSL) is a field-based expert on scientific data, products and trials, responsible for engagement with medical stakeholders at Clinical Trial Centers (Kidney Transplant Studies) across the region.The MSL will represent and reflect client values as a science-driven, patient-centric organization.The MSL is critical in understanding the management of diseases of interest, mapping the patient journey, identifying unmet medical needs, data gaps and areas of collaboration.The MSL will work closely wit the Kidney Transplant Clinical Trial Teams.While the focus will be on the region, the function will also support activities and projects across the EMEA region.ROLES AND RESPONSIBILITIES Expert medical resource and ambassador Maintain the highest scientific and medical expertise of all relevant diseases and, products; be acknowledged internally and externally as an expert.Focus lies on the Clinical Trials we are conducting in the Transplant TA (DGF and AMR with empa and efgar respectively) Identify and develop productive relationships and collaborations with all relevant stakeholders, including healthcare professionals, professional organization.Support the development and implementation of the kidney transplant site engagement plan to advance client objectives.Help shape the position of the client in the region.Maintain a high level of knowledge of and appropriately implement current local pharmaceutical regulation and ensure implementation of client policies and procedures.Scientific/medical exchange and education, and insight generation Ensure timely and informative scientific/medical exchanges with external stakeholders that accurately reflect scientific data.Deliver high quality scientific/medical education in a variety of settings, including related to diseases of interest, clinical studies (focus on our DGF trial and in 2nd line AMR Trial), investigational products and any future licensed products.Obtain feedback that can be disseminated throughout the organization.Coordinate the timely and appropriate response to internal and external Medical Information enquires, utilizing client medical information resources and in line with regulatory requirements
