Senior Clinical Trial Manager, Interventional Oncology and Embolization (IO&E)
Additional Location(s): US-MN-Maple Grove; US-MA-Marlborough
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:As a Senior Clinical Trial Manager in Boston Scientific's Interventional Oncology and Embolization (IO&E) team, you will play a pivotal role in advancing our oncology pipeline by leading early feasibility clinical trials. This position offers a unique opportunity to apply agile, innovative approaches to accelerate the development of novel cancer therapies. You will be responsible for leading cross-functional teams through the design and execution of complex, global studies that drive forward early-phase clinical evidence. Work model, sponsorship, relocation: At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local office at least three days per week. Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time. Relocation assistance is not available for this position at this time. Your responsibilities will include:
- Leading and driving cross-functional project teams in the planning, execution, and management of strategic and operational aspects of interventional oncology clinical trials
- Directing and developing clinical studies/programs in alignment with strategy, timelines, budgets, and regulatory guidelines
- Managing and tracking development of project documentation, manuals, systems, plans, and regulatory submissions
- Collaborating with external physicians and key opinion leaders (KOLs) to advance clinical strategy and execution
- Overseeing clinical trial project budgets-up to 25% depending on the project lifecycle-including monthly reconciliation, variance analysis, and forecasting
- Providing direction to Contract Research Organizations (CROs) and clinical vendors to ensure high-quality deliverables
- Ensuring audit readiness across all study activities and documentation
- Proactively identifying, assessing, and mitigating clinical study risks
- Developing and presenting study progress, data, and risk insights to internal leadership
- Offering clinical input into product development and representing Clinical on cross-functional teams
- Traveling domestically up to 10-25%, as required
- Bachelor's degree and minimum of 5 years' oncology-related experience (or equivalent combination of education and experience)
- Minimum of 1 year experience conducting early feasibility oncology clinical research studies
- Minimum of 1 year experience managing projects or clinical trials
- Minimum of 1 year experience in clinical trial financial and budget management
- Minimum of 1 year experience working with CROs, clinical vendors, and outsourced operations
Preferred qualifications:
- Experience in solid tumor studies, medical device trials, or drug development
- Prior involvement on product development teams
- Ability to apply creative thinking to problem-solving and process improvement
- Strong strategic thinking with demonstrated ability to independently align activities with program and business goals
- Proven collaboration and influencing skills across global cross-functional teams
- Adaptability and resilience in navigating change and ambiguity
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