Medical Affairs Director (MD)

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life Clinical Research & Medical Sciences Director South Korea Reports to: Senior Director Clinical Research & Medical Sciences, Asia RLM and ANZ Careers That Change Lives Join a mission-driven industry leader in medical technology and solutions to help drive innovation and transform the healthcare landscape. As Clinical Research & Medical Sciences Director you will oversee both clinical and medical sciences aspects of running the medical organization in the South Korea. Reporting to Senior Director Clinical Research & Medical Sciences, you will lead the development and execution of clinical research and medical sciences agenda in S. Korea to enable patient access to innovative medical technologies. A Day in Life   Provides Clinical/Medical Leadership at Business Reviews and discussions with the respective Country Leaders. As a Leader within the Korea organization, contributes to the development of a Clinical & Medical affairs strategy and execute them in the country. Is seen as the Voice of the Patient and the HCP. Provides Strategic Leadership for the development of Clinical strategy across OUs relevant to the region in Medtronic sponsored studies, Collaborative Research and ERPs including execution of Clinical Research and Medical Affairs. Ensures that the studies are scientifically valid and meet all relevant regulatory requirements and be conducted within ethical guidelines. Leads execution for both local and global studies, manages clinical research projects across Medtronic therapies across multiple businesses. Ensures that all clinical studies are published based on a fair assessment of the safety and efficacy of the tested product (s) and attainment of product approvals in a timely matter. Partners with the OUs/Marketing regionally to seek insights and disseminate the published data both globally and regionally. This may be done through Advisory Boards (ABs) to seek advice, Focus Group Discussions (FGDs), Continuing Medical Education (CMEs), Round Table Discussions (RTDs), and webinars for safe and effective use of our products. Partners with Regulatory to contribute and partnering to implement regulatory strategies to obtain timely product approvals form worldwide regulatory bodies. Develop the Healthcare Professional (HCPs) and Key Opinion Leaders network and lead a strategic partnership and engagement. Develops and maintains a deep knowledge and understanding of the science behind our products and is seen as an internal expert. To also act as a Speaker in scientific meetings as the voice of the company. Responsible for the governance and compliance within the region. Ensures that all activities are executed as per the Medtronic Business Code of Conduct and local laws and regulations. Utilizes advanced subject matter expertise to provide medical input to various functions (General Management, Global Strategy & Portfolio Management, Business Development & Licensing, Research & Development, & Marketing) and Organizational Units to facilitate insightful decision-making and enable achievement of business objectives. Ensures effective objective value propositions are developed and articulated for Medtronic technologies to stakeholders (patients, health care providers, payers, government agencies, health technology assessment organizations, public) through appropriate channels. Responsible to interpret clinical trials/research, establishes and approves scientific methods for design and implementation of clinical protocols, and final reports.