Boston Scientific
Principal Scientific Affairs Specialist, Drug Eluting Technologies
Boston Scientific, Osseo, Minnesota, United States, 55311
Principal Scientific Affairs Specialist, Drug Eluting Technologies
Work mode: Hybrid Onsite Location(s): Maple Grove, MN, US, 55311 About the role: The Principal Scientific Affairs Specialist, Drug Eluting Technologies is an individual contributor role within the Interventional Cardiology Therapies (ICTx) SciAffairs team that specializes in device-based drug elution techniques and technologies. In this role, you will drive strategic initiatives in medical science and medical education that are directly related to the various drug eluting product lines within the BSC ICTx portfolio. You will become the subject matter expert in drug eluting technologies responsible for driving scientific investigations, generating and disseminating medical and scientific data, analyzing competitive landscapes from a scientific perspective, and developing specialized scientific content that supports, informs, and influences ICTx product strategy. You will provide professional and timely cross-functional support to Global R&D, Clinical, Marketing, Medical Affairs, and Medical Education teams. Work Mode: This is a Maple Grove, Minnesota-based hybrid role with 3 days in-office when not traveling for customer engagements. Relocation Assistance: Relocation assistance is not available for this position at this time. Visa Sponsorship: Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Your responsibilities will include: Plan, develop, and execute clinical and scientific data generation/dissemination strategies Develop a deep understanding of, and stay up-to-date on, the clinical science and other relevant, industry-wide scientific content related to drug eluting ICTx product lines Contribute to the development of education and support tools to be used by both internal and external global teams Create a library of educational materials aligned with organizational strategic objectives, clinical strategies, and commercial priorities Partner closely with regional medical affairs and medical education colleagues to ensure global impact of activities Develop, facilitate, execute, and track longitudinal strategic publication plans in close partnership with clinical affairs, R&D, and other internal stakeholders Contribute to non-IDE publication related activities associated with drug eluting technology product lines Regularly summarize and disseminate up-to-date study results and key messaging points to internal and external teams Identify drug eluting technology users and KOLs, develop (and execute) engagement strategies in partnership with other functional partners, and provide customer-facing feedback associated with KOL needs Engage with scientific societies, external influencers, and internal stakeholders in support of drug eluting technology strategies Partner closely with medical education to identify, and/or organize, symposia opportunities for internal partners and steer presentation topic discussions Required Qualifications: Minimum of 3 years relevant experience in medical device industry, or 1+ years with advanced medical or scientific degree Fluency in understanding and interpretation of clinical data Ability to travel up to 30%, both domestically and internationally. Proven collaborative track record Customer facing experience, KOL engagement/relationship building necessary Ability to quickly digest/interpret/explain scientific data Strong interpersonal skills to enable cross function and cross franchise success Strong presentation and communication skills High sense of urgency and commitment to execution Must have the ability to manage simultaneous priorities, changing deadlines, and limited resources Preferred Qualifications: Experience in scientific publication Experience with drug eluting technologies Advanced medical or scientific degree Previous experience in a global role
Work mode: Hybrid Onsite Location(s): Maple Grove, MN, US, 55311 About the role: The Principal Scientific Affairs Specialist, Drug Eluting Technologies is an individual contributor role within the Interventional Cardiology Therapies (ICTx) SciAffairs team that specializes in device-based drug elution techniques and technologies. In this role, you will drive strategic initiatives in medical science and medical education that are directly related to the various drug eluting product lines within the BSC ICTx portfolio. You will become the subject matter expert in drug eluting technologies responsible for driving scientific investigations, generating and disseminating medical and scientific data, analyzing competitive landscapes from a scientific perspective, and developing specialized scientific content that supports, informs, and influences ICTx product strategy. You will provide professional and timely cross-functional support to Global R&D, Clinical, Marketing, Medical Affairs, and Medical Education teams. Work Mode: This is a Maple Grove, Minnesota-based hybrid role with 3 days in-office when not traveling for customer engagements. Relocation Assistance: Relocation assistance is not available for this position at this time. Visa Sponsorship: Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Your responsibilities will include: Plan, develop, and execute clinical and scientific data generation/dissemination strategies Develop a deep understanding of, and stay up-to-date on, the clinical science and other relevant, industry-wide scientific content related to drug eluting ICTx product lines Contribute to the development of education and support tools to be used by both internal and external global teams Create a library of educational materials aligned with organizational strategic objectives, clinical strategies, and commercial priorities Partner closely with regional medical affairs and medical education colleagues to ensure global impact of activities Develop, facilitate, execute, and track longitudinal strategic publication plans in close partnership with clinical affairs, R&D, and other internal stakeholders Contribute to non-IDE publication related activities associated with drug eluting technology product lines Regularly summarize and disseminate up-to-date study results and key messaging points to internal and external teams Identify drug eluting technology users and KOLs, develop (and execute) engagement strategies in partnership with other functional partners, and provide customer-facing feedback associated with KOL needs Engage with scientific societies, external influencers, and internal stakeholders in support of drug eluting technology strategies Partner closely with medical education to identify, and/or organize, symposia opportunities for internal partners and steer presentation topic discussions Required Qualifications: Minimum of 3 years relevant experience in medical device industry, or 1+ years with advanced medical or scientific degree Fluency in understanding and interpretation of clinical data Ability to travel up to 30%, both domestically and internationally. Proven collaborative track record Customer facing experience, KOL engagement/relationship building necessary Ability to quickly digest/interpret/explain scientific data Strong interpersonal skills to enable cross function and cross franchise success Strong presentation and communication skills High sense of urgency and commitment to execution Must have the ability to manage simultaneous priorities, changing deadlines, and limited resources Preferred Qualifications: Experience in scientific publication Experience with drug eluting technologies Advanced medical or scientific degree Previous experience in a global role