Boston Scientific · 15 hours ago
Clinical Risk Evaluation Intern
Boston Scientific is a leader in medical science dedicated to solving significant health industry challenges. The Clinical Risk Evaluation Intern will work collaboratively to develop global evidence-based clinical strategies for cardiology medical devices, focusing on regulatory approval processes and documentation synthesis.
Health CareMedicalMedical Device
Responsibilities
Gain exposure to the manufacturing and development process for Class III medical devices in the cardiology space
Develop foundational knowledge of regulatory and Quality Management System (QMS) requirements for medical devices, including how manufacturers ensure safety, performance, and benefit
Collaborate with cross-functional teams, including Regulatory Affairs, Clinical Trials, Clinical Risk, Research and Development, and Design Assurance/Quality
Conduct state-of-the-art assessments for specific medical conditions treated or diagnosed by Cardiac Rhythm Management (CRM) devices, such as Cardiac Leads, Pacemakers, Subcutaneous Implantable Cardioverter-Defibrillators (S-ICDs), Transvenous Implantable Cardioverter-Defibrillators, and Cardiac Resynchronization Therapy – Defibrillators (CRT-D)
Support experienced Clinical Risk specialists in achieving project milestones and deliverables
Contribute to ongoing monitoring and analysis of literature via screening published literature for relevant articles and extracting key safety, performance, and benefit data utilizing DistillerSR
Assist in the development and maintenance of key Clinical Risk documentation, including Clinical Evaluation Plans/Reports and Post-Market Clinical Follow-Up Plans/Reports
Review documents for accuracy and completeness prior to submission to regulatory bodies
Participate in Clinical Risk and project team meetings, providing support for preparation, documentation, and follow-up activities
Qualification
Required
Must graduate between Fall 2026 – Spring 2027
Currently pursuing a bachelor's or graduate level degree majoring in Biomedical Engineering, Bioengineering, or Life Sciences
Must be able to commit to one of the following full internship program periods: May 18th – August 7th OR May 26th – August 14th
Must be eligible to work in the U.S. without company sponsorship, now or in the future, for employment-based work authorization
Must have reliable transportation to and from the Arden Hills, MN, Boston Scientific Corporate location
Must have at least 3 months or more experience reviewing clinical data, evaluations, or trials
Preferred
Strong analytical and quantitative skills
Excellent written and verbal communication skills
Strong computer and MS Office skills
Ability to work independently while contributing to the team goals
Attention to detail and good organizational skills, including balancing multiple projects
Experience with reading and analysis of primary scientific literature
Familiarity with or exposure to clinical trial principles and design
Basic understanding of disease states, medical treatments, human and/or animal anatomy and physiology and how they relate to products
Experience with data analysis and extraction databases
Related work/intern experience
Benefits
Relocation and housing assistance may be available to those who meet the eligibility criteria.
Company
Boston Scientific
Boston Scientific is a medical technology company that designs and develops medical devices to diagnose and treat a wide range of condition.
Funding
Current Stage
Public CompanyTotal Funding
$10.02B2025-02-21Post Ipo Debt· $1.58B
2024-02-22Post Ipo Debt· $2.17B
2022-03-04Post Ipo Debt· $3.28B
Recent News
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2026-01-20
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2026-01-20
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