Job Description The role can be based anywhere in Europe and may require international travel to various local markets as needed. We are a research driven biopharmaceutical company. Our mission is built on the simple premise that if we follow the science and that great medicines can make a significant impact on our world. We believe that a research driven enterprise dedicated to world class science can succeed by inventing medicine and vaccine innovations that make a difference for patients across the globe. The Regional Director Medical Affairs (RDMA) is responsible for driving execution of scientific & medical affairs plans for pulmonary hypertension in defined countries in Europe. They are impactful members of regional cross functional teams, including regional Commercial, Center of Real World Evidence (CORE), Policy, and Market Access. They engage with their network of scientific leaders in their region. This is a regionally based position (i.e., residing in one of the affiliates of the region or regional hub) in our Company Research Laboratories Global Medical and Scientific Affairs (our Research & Development Division GMSA). Responsibilities and Primary Activities: Guides country our Research & Development Division GMSA staff to execute the annual scientific & medical plan for their assigned TA. Chairs the Regional Medical Affairs Team to ensure execution of agreed medical tactics and leverage best practices. Ensures scientific exchange is aligned with the global scientific communications platform. Partners with regional Commercial, regional Center of Real World Evidence (CORE), regional Policy, and regional Market Access to drive development and execution of region plans. Consolidates actionable medical insights from countries in their region. Engages with a network of contracted Scientific Leaders (SL) and other key stakeholders (therapeutic guideline committees, payers, public groups, government officials, medical societies) from their region. Supports, as regional TA expert, affiliates staff in engagement with their national scientific leaders. Organizes regional expert input events to answer Our Companys questions regarding how to implement new indications: advisory boards and expert input forums. Organizes regional symposia and educational meetings. Supports countries with the development of local data generation study concepts and protocols. Reviews investigator initiated study proposals prior to headquarters submission (ex USA). Manages regional programs (patient support, educational or risk management) to support appropriate and safe utilization of Our Companys medicines. Required Qualifications, Skills & Experience: Minimum: MD, PhD or PharmD (MD preferred) and recognized medical expertise in the therapy area. Five+ years experience in country/region Medical Affairs. Strong prioritization and decision making skills. Able to effectively collaborate with partners across divisions in a matrix environment. Excellent interpersonal