Senior Clinical Trial Specialist

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 Senior Clinical Trial Specialist is responsible for driving and managing the execution of global Peripheral Interventions clinical studies worldwide with guidance from clinical project managers in support of the organization’s business objectives for product development and/or commercialization.

 

Work Mode:
At Boston Scientific, we value collaboration and synergy. This role follows a hybrid work model requiring employees to be in our local Arden Hills, MN or Maple Grove, MN office at least three days per week.

 

Relocation Assistance:
Relocation assistance is available for this position.

 

Visa Sponsorship:
Boston Scientific will not offer sponsorship or take over sponsorship of an employment visa for this position at this time.

 
Your responsibilities include:

• Supports management of the project team in the planning, execution and management of all operational aspects of clinical trials and clinical evidence generation projects.
• Supports execution of clinical trials and/or clinical programs worldwide in accordance with strategy, project plans, approved budget and resource allocations following applicable regulatory and standard operating procedures.
• Collaborates with the project team on development of internal and external project materials, processes, manuals, plans, committees, clinical systems and sponsor required regulatory submissions.
• Proactively manages clinical data compliance, including data review and interpretation for early identification of trends.
• Ensures the project team maintains a continuous state of audit readiness.
• Leads the proactive identification, assessment, and management of clinical trial risks, in collaboration with the project team.
• Assists with authoring clinical trial reports.
• Provides progress updates as needed.
• Additional clinical trial activities as required and directed.

 
Required Qualifications:

• Bachelor’s degree and 5+ years clinical research and/or clinical trial experience required
• Ability to work collaboratively and influence a broad range of global stakeholders
• Experience with Contract Research Organization (CRO) collaboration and oversight

• Peripheral Interventions clinical trial experience desired

Preferred Qualifications

• Ability to respond flexibly and positively under conditions of uncertainty or change
• Ability to apply comprehensive knowledge and experience to resolve complex issues in creative ways
• Wide-range of clinical trial operations experience strongly preferred (ex: Site Management, Monitoring, Data Management, and/or Safety)

 

 

 

Requisition ID: 614586 

Minimum Salary: $ 82600 

Maximum Salary: $ 156900 

 

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) – see www.bscbenefitsconnect.com—will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

 

Compensation for non-exempt (hourly), non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift different