Senior Clinical Trial Manager - Interventional Oncology & Embolization

Additional Location(s):  N/A

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:
The Sr. Clinical Trial Manager Oncology, will support the IO&E team focused on the development of oncology clinical trials. In this role, you will have responsibility for leading cross-functional clinical teams in the execution of Early Feasibility Studies (EFS) 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.

 

Work Mode:

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.

 

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:

• Leads and drives the project team in the planning, execution and management of strategic and operational aspects of clinical interventional 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 travel up to 10 to 25%, 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 early feasibility 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:

• Solid tumor, medical device and/or drug development experience
• Experience with product development teams preferred
• 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 change

 

 

 

Requisition ID: 610426 

Minimum Salary: $ 122100 

Maximum Salary: $ 23200