Senior Medical Director - Watchman

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: 

At Boston Scientific, as a Senior Medical Director, Watchman you will play a pivotal role in influencing the advancement of Watchman therapies across the globe. Your expertise will guide our clinical strategy, working closely with our research and development team and key opinion leaders to help ensure Watchman remains innovative, safe, and effective for an increasing number of patients needing left atrial appendage closure.  

 

Work Mode

This role follows a hybrid work model, requiring employees to be in a 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.

 

Your responsibilities will include:

• Scientific Guidance and Collaboration: Provide medical and scientific guidance to internal and external stakeholders, including clinical trials teams, functional units, study investigators, and regulatory agencies. 
• Collaborate with cross-functional teams to ensure alignment with medical objectives for the Watchman team
• Operational Support and Oversight: Participate in clinical trial planning, protocol development, and investigator selection. 
• Train internal and external personnel on medical aspects related to trial conduct. 
• Therapeutic Area Expertise: Leverage your medical expertise throughout the device life cycle and Serve as a medical advisor for regulatory matters. 
• Participate in the evaluation of adjacent business development opportunities. 
• Innovation and Technology Integration: Contribute to the application of new technologies in solving complex medical challenges. 
• Provide clinical due diligence for new product development and business initiatives. 
• Clinical and Scientific Communication: Write and edit clinical and scientific reports, and review and approve educational materials
• Ensure accuracy and consistency in clinical trial protocols. 
• Develop and maintain relationships with key thought leaders in the medical community preferably interventional cardiology
• Participate in local, national, and international medical conferences. 

 

Required qualifications: