Medical Advisor, Italy

**Location(s)**:**Rome, Italy **Level of position**:**Associate Director **Position type**:**70% Office-based, 30% Field-based (Or office-based with 30% business travel) **Reporting Line**:**The position reports to the Country Medical Lead **How will your role help us transform hope into reality?** The Medical Advisor role at Blueprint Medicines is a critical position within the organization, responsible for providing medical, scientific and strategic expertise to support Italy's development and commercialization programs. As a Medical Advisor, you will play a key role in driving the success of Blueprint's mission to improve and extend the lives of as many patients as possible through precision therapy. You will be a reliable bridge between clinical research, market access and commercialization and within the overall organization building strong relationships and collaboration with external and internal stakeholders. As a Medical Advisor you will be living and sharing our core values and will be driven by the pursuit of new ideas, new innovations, and new ways of thinking to help advancing a diverse portfolio of innovative therapies for mast cell disorders, including systemic mastocytosis and chronic urticaria, and cancer, including breast cancer and other solid tumors. At Blueprint we place great emphasis on the "How" of our daily job that aligns with our core values and is implemented through the following competencies: You will also have the opportunity to develop, learn and improve your strategic prioritization attitude and your effect as a potential impact multiplier. **What will you do?** - Proactively manage KOLs in the interest of Blueprint at the country level through your deep knowledge of the country's KOLs landscape, - Establish and maintain strong relationships with KOLs, HCPs and PI's and be recognized by them as Blueprint's reference point and connector. - Represent the company at relevant medical conferences and symposia. - Foster the establishment and maintenance of local scientific advisory boards, round tables, expert meetings and scientific advocacy development. - Closely cooperate with the country Medical Lead supporting the execution of medical plans as well as taking over the co-ordination of specific scientific projects. - Cultivate a trustful and effective two-way collaboration with MSLs, supporting their presence in the field. - Provide a source of key medical knowledge on the company's products and ensure that all regulatory requirements are met and aligned with local and Global standards. - Maximize your skills in critically analyzing and interpreting clinical trial data, real-world evidence, and scientific literature. You will communicate the clinical implications of data and contribute to the development of scientific publications and presentations. - Collaborate in insights collection and analysis to be translated into guidance for internal colleagues from different functions across the company. - Build strong collaborative relationships with cross functional teams to ensure alignment with medical and business objectives. - Works closely with local, regional and global market access colleagues in preparing strong price and reimbursement dossiers that will be tested extensively with medical experts and national leaders. May also have to represent it to reimbursement authorities. - Actively support upcoming launches by the means of Blueprint Medicines company sponsored symposia and other activities. - Reviews and signs off local educational and promotional material as the responsible information officer for the corresponding indication and of clinical trial treatment plans and protocols of Phase IV projects in line with local compliance regulations. Provide medical input into promotional campaigns and provide medical input in the health benefit discussion related to new products. - Develop and deliver medical education programs for internal teams, healthcare professionals, and other stakeholders. - Collaborate closely with International Medical teams to identify key data/material gaps and help in developing medical material and resources. - Support interventional and non-Interventional clinical trials in close collaboration with Clinical development, Clinical Operations and Global Medical Affairs teams. Ensure a strategic approach to such programs, and the development of clinical data to support the appropriate use of the Company's products. - Ensures that Investigator Initiated Research studies are in line with the global strategy. Helps to detect need for and enables Real World Evidence generation when required for advancing therapeutic area a/o for access needs. **What minimum qualifications do we require?** - Advanced Clinical/Science degree or professional credentials required (PhD, MD, PharmD, MSc). - 3+ years of experience in the biotech or pharmaceutical industry in a similar role. - Excellent communication and presentation skills, with the ability to effectivel