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Boston Scientific Senior Clinical Trial Manager, Oncology in Maple Grove, Minnesota

Additional Location(s):US-MN-Maple Grove; US-AL-Anniston; US-AL-Auburn; US-AL-Birmingham; US-AL-Mobile/Dothan; US-AL-Montgomery; US-AL-Northern/Huntsville; US-AL-Tuscaloosa; US-AR-Eastern; US-AR-Fayetteville; US-AR-Fort Smith; US-AR-Little Rock; US-AZ-Flagstaff; US-AZ-Lake Havasu; US-AZ-Phoenix; US-AZ-Tucson; US-AZ-Yuma; US-CT-Danbury/Bridgeport; US-CT-Hartford; US-CT-New Haven; US-CT-Stamford; US-DC-Washington; US-DE-Delaware; US-FL-Daytona; US-FL-Ft. Lauderdale; US-FL-Ft. 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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. This is a remote eligible role within the country About the role: The Clinical Trial Manager/Senior Clinical Trial Manager - Oncology, will support the Interventional Oncology & Embolization (IO&E) team focused on the development of Interventional Oncology & Embolization clinical trials. In this role, you will have responsibility for leading cross-functional clinical teams in the design, planning, and execution of Phase II-III pivotal clinical trials, with a focus on agility, learning, and creative thinking to move forward quickly and identify new and breakthrough cancer therapies for our pipeline. Your responsibilities will include: Leads and drives the project team in the planning, execution and management of all operational aspects of clinical oncology trials Leads, directs develops, and executes clinical studies and/or programs worldwide in accordance with strategy, project plans, approved budget and resource allocations following applicable regulatory and standard operating procedures Tracks development of and collaborates with the project team on all internal and external project materials, processes, manuals, plans, committees, study systems and all sponsor required regulatory submissions Interacts and collaborates with external physicians and key opinion leaders (KOLs) Responsible for overall clinical trial project budget and maintenance up to 25%, dependent on project life cycle. Includes, monthly maintenance, routine and quarterly variance review, forecasting and strategic planning within accepted variance targets Provides direction and oversight to Contract Resource Organization (CROs) and other clinical vendors Ensures the project team maintains a continuous state of audit readiness In collaboration with the project team, leads the proactive identification, assessment, and management of clinical study risks Supports development of presentations and/or presents on study progress, data, outcomes and risks to leadership Provides clinical input to product development activities; represents Clinical on product development team Domestic and international travel up to 10 to 15%, as required Required qualifications: Bachelor's degree and 5+ years of oncology-related work experience or an equivalent combination of education and work experience Previous experience performing oncology clinical research studies, 1 - 3 years Project/trial management experience, 1 - 3 years Financial acumen and budget management experience, 1 - 3 years Experience with CROs, other clinical vendors, and outsourced operations, 1 - 3 years Preferred qualifications: Ability to Apply new ways of looking at problems, processes, or solutions to generate new ideas, approaches, and initiatives Maintain strategic perspective and independently implement action plans and align activities with project, program and business objectives without significant supervision Effectively collaborate and influence a broad range of global stakeholders Respond flexibly and positively under conditions of uncertainty or... 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

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