Additional Location(s):US-MN-Arden Hills; US-MA-Marlborough; US-MN-Maple Grove Diversity - Innovation - Caring - Global Collaboration - Winning Spirit- High Performance At Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we'll help you in advancing your skills and career. Here, you'll be supported in progressing - whatever your ambitions. About the role: Boston Scientific is seeking an experienced Cardiac Electrophysiologist looking to transition into the medical device industry. This Global Medical Director (GMD) position for our Rhythm Management Division (with focus on our Cardiac Diagnostic Therapies and Services) is a key medical leadership role which offers the opportunity to leverage your therapeutic area expertise and procedural experience to support Boston Scientific's mission of developing and sustaining the best possible therapies and services for the patients we serve. This Global Medical Director acts as an advocate for the patient and a champion for the optimization of medical device safety throughout the product's lifecycle (pre-clinical, clinical and post-market), and a key subject matter expert involved in the development of multiple aspects of these technologies. This Global Medical Director will play a pivotal role in shaping Boston Scientific's Cardiac Diagnostics Services business and our Rhythm Management Portfolio in general. This position requires profound therapeutic area knowledge in cardiac electrophysiology, alongside substantial expertise in patient management and procedural skills. As part of our medical team, you will champion the advancement of safe devices and services and ensure the effective communication of their benefits and risks in a thorough and pertinent manner. This also involves qualitative and quantitative application of scientific evidence and medical analysis to promote patient safety, balance risk with benefit, guide strategy, and drive innovation. This key medical leadership role carries responsibility for ensuring that rigorous, proactive medical input is provided across all areas of the business and serves as the voice of the physician and patient in the clinical study and commercial application of our technologies. The ultimate goal of this role is to safeguard at all times patient safety. . The Global Medical Director works in a collegial, collaborative environment with medical colleagues within the team, division and cross-divisionally; and partners closely with cross-functional partners to deliver the best possible quality to Boston Scientific patients. Your responsibilities will include: As an active member of and leader within a medical and patient safety team comprising medical, patient safety, clinical trials operations safety and cardiac diagnostics services, the GMD exhibits high levels of ethics and accountability and acts as a key advocate for our function to influence internal and external stakeholders in matters of medical device safety. Provides thorough/evidence-based medical guidance, operational support, oversight, and therapeutic area expertise for a range of workstreams and internal customers encompassing the span of the entire product lifecycle as it relates to device safety and performance. Main spheres of activity include new product development and risk management, clinical trial safety and medical monitoring, post-market surveillance activities, assessment of device performance signals, and provision of general medical subject matter expertise. Supported teams include clinical trials, clinical evidence, quality, Research and Development (R&D), regulatory affairs, post-market surveillance, marketing, business development, and other functional units. Engages compliantly on behalf of Boston Scientific in external interactions with study inv stigators, regulatory bodies, Key Opinion Leaders (KOLs), physician customers, professional societies and advisory boards on matters of device performance, medical safety and medical matters in general as they relate to the therapies and services provided by Boston Scientific. Interacts with independent committees such as clinical event committees (CEC) and data monitoring committees (DMC), ensuring exchange of information with these committees is transparent and adequate to meet objectives of safety oversight. Provides hands-on operational support and oversight to teams regarding clinical trial planning, clinical protocol development, investigator selection, training of internal and external personnel, medical monitoring for patient safety and trial conduct, individual and aggregate clinical trial safety review, data analysis and interpretation, quality control, and presentation/publication. Provides specialized therapeutic area expertise throughout the device life cycle, including medical input into risk management, Clinical Evidence Reports (CERs), Summaries of Safety and Clinical Performance, product complaints, vigilance reports, health risk assessments, field safety communications, and serves as a medical advisor for regulatory issues and in the creation of instructional material/labeling to ensure safe use of medical devices. Provides direct medical input into post-market trending and safety signal detection, assessment, management and reporting. Liaises with Boston Scientific field personnel and Health Care Providers (HCPs) to help assess significant adverse events. Advises on failure investigations and provides medical guidance in assessing health hazards posed by device failure. Implements experience-based understanding of medical risk and benefit to arrive at objective assessments of health risk. Monitors and assesses adverse events to determine the escalation of safety issues for communication and action to senior leadership. Regularly interacts with senior management concerning significant and emerging safety matters. Provides independent review, authorship and approval of a range of clinical, scientific and safety reports used for safety and performance assessment in various quality, risk management, clinical trial and clinical evidence processes for risk management, post-market surveillance and regulatory submission. Reviews and approves educational and promotional materials.Also reviews and edits clinical trial protocols to ensure accuracy, consistency with standard of care and relevant safety standards and regulations, logistical ease, and internal consistency with BSC Quality Policies. Contributes to internal development and assessment of novel technologies, provides strategic input for business development teams, and provides medical evaluation in due diligence and operational support for integration of acquired technologies. Plays a key role in the integration of acquired technologies (including processes and clinical trials) into Boston Scientific Rhythm Management. Contributes to training and mentorship of medical and non-medical personnel within the division who have safety-focused or adjacent roles. Required qualifications: Minimum of 5 years of clinical experience in the practice of cardiac electrophysiology in a clinical environment managing patients and performing complex cardiac electrophysiology procedures. Expert knowledge of and experience in medical and interventional management of complex cardiac arrhythmias. Demonstrated leadership responsibilities and strong interpersonal skills with experience working effectively in a team/matrix environment. Strong analytical skills and attention to detail. Excellent communication... For full info follow application link. Boston Scientific is an Equal Opportunity Employer Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Disability, Veteran