SpringWorks: (Senior) EU Medical Affairs Manager Ogsiveo (all genders, Part time/Full time possible)

<p> </p> <p><span><span>Work Your Magic with us!  </span></span></p> <p> </p> <p><span><span>Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.  </span></span></p> <p> </p> <p><span><span>United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.</span></span></p> <p> </p> <p><span>SpringWorks Therapeutics, a healthcare company of Merck KGaA, Darmstadt, Germany, is a commercial-stage biopharmaceutical company dedicated to improving the lives of patients with rare tumors.   </span></p> <p><span>We developed and are commercializing the first and only FDA and EC approved medicine for adults with desmoid tumors and the first and only FDA and EC approved medicine for both adults and children with neurofibromatosis type 1 associated plexiform neurofibromas (NF1-PN). </span></p> <p><span>At SpringWorks, we are committed to finding answers people with rare tumors need. We thrive in an atmosphere of passion and tenacity, fueled by the excitement of the possibilities science may unlock and driven to work with urgency because of the importance of our work. We value authenticity because diverse backgrounds, cultures, styles and abilities can only help us find the answers that people with rare tumors are looking for. </span></p> <p><span><strong>Your Role:</strong> The Senior Medical Director EU will lead the development and execution of the European medical strategy for our product-specific late-phase development programs. This role demands a scientifically sound approach, ensuring compliance with all relevant regulations and internal SOPs. The Senior Medical Director will also manage Medical Affairs resources effectively to support various plans and projects.</span></p> <p><span>The Senior Medical Director EU is also responsible for line management of Medical Rare Tumours (RT) teams within their allocated countries, and oversight of strategic and tactical activities within those countries. This role will work cross functional with other European Medical Affairs Directors to ensure product level strategic guidance within the allocated countries. Exact Geographic scope is TBC.</span></p> <p> </p> <p><span><strong>Key Responsibilities will include:</strong></span></p> <ul type="disc"> <li><span>Serve as the internal European expert on disease states, products, and competitive intelligence for assigned compounds/indications.</span></li> <li><span>Collaborate with the Medical Strategy team to develop the global product strategy and lead the European medical affairs strategy and tactical plans.</span></li> <li><span>Oversee life cycle management of compounds in Europe, including Phase IV studies and registries.</span></li> <li><span>Drive the execution of product-specific European launch strategies in partnership with cross-functional teams.</span></li> <li><span>Develop and execute advisory boards, publication plans, and educational activities at both European and national levels.</span></li> <li><span>Partner with global functions for the European aspects of the investigator-initiated research (IIR) program.</span></li> <li><span>Collaborate with Patient Advocacy leads on product-related activities.</span></li> <li><span>Provide scientific and medical support for HEOR studies and reimbursement activities.</span></li> <li><span>Represent Medical Affairs with internal and external stakeholders in Europe.</span></li> <li><span>Line manage and coach direct reports within allocated countries.</span></li> <li><span>Participate in European Medical Leadership team and relevant cross-functional leadership meetings.</span></li> </ul> <p><span><strong> </strong></span></p> <p><span><strong>Who you are: </strong></span></p> <ul> <li><span>MD, PhD, or PharmD</span></li> </ul> <ul type="disc"> <li><span>12+ years of industry experience, with at least 5 years in medical affairs function.</span></li> <li><span>Must have experience in regional medical affairs, not single market oversight alone.</span></li> <li><span>Rare disease experience, with oncology knowledge also desirable.</span></li> </ul> <ul type="disc"> <li><sp