Medical Safety Specialist III - Neuromodulation
About The Position
This role manages surveillance processes across a wide range of Boston Scientific Neuromodulation products and disease states including Parkinson's disease, Dystonia, Essential Tremor, and Chronic Pain. The position is responsible for completing accurate, timely, and consistent medical assessments of adverse and potential adverse events to ensure safety vigilance throughout the total product lifecycle. This individual will collaborate with cross-functional partners including Clinical, Regulatory, Quality, and the Complaint Management Center, and will work alongside Medical Safety colleagues under the supervision of the Medical Director. 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.
Requirements
- Bachelor's degree or equivalent in a healthcare-related field (e.g., registered nurse, physician assistant, nurse practitioner).
- Minimum of 5 years' experience in direct patient care, preferably in a hospital, interventional setting, or outpatient surgical center.
- Demonstrated ability to work independently, understand complex medical information, and lead projects or assignments proactively.
Nice To Haves
- Post-market surveillance experience in the medical device industry.
- Experience with neurosurgery or interventional pain products.
- Experience in clinical or scientific research, preferably involving medical devices.
Responsibilities
- Provide medical support for neuromodulation medical devices within the Boston Scientific Neuromodulation division.
- Apply clinical knowledge and experience to a wide range of neuromodulation products and indications.
- Analyze data from multiple sources (e.g., complaints, Medical Device Reports), identify potential safety issues, and contribute to trend analysis.
- Conduct medical review and assessment for individual case safety reports, aggregate reports, literature, risk management, and other required documentation.
- Perform clinical review of hazard analyses and related risk documentation.
- Represent Medical Safety in cross-functional team meetings such as complaint trend reviews.
- Escalate potential patient safety issues for decision-making and/or action by senior leadership.
- Apply working knowledge of global medical device regulations and standards.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees
