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Elucid

Director of Regulatory

Posted 12 Days Ago
Be an Early Applicant
In-Office
Boston, MA, USA
175K-225K Annually
Senior level
In-Office
Boston, MA, USA
175K-225K Annually
Senior level
Lead global regulatory strategy and submissions for AI-enabled cardiovascular medical imaging software. Manage FDA, EU MDR, and international regulatory pathways from pre-submission through post-market lifecycle management. Partner with Quality, Engineering, Clinical, Commercial, and Product teams to ensure compliant product development and clearance. The role also includes people management, cross-functional guidance, and translating complex medical device regulations into actionable execution plans.
The summary above was generated by AI
We are a rapidly growing, Boston-based medical technology company using AI to enable clinicians to make informed decisions on cardiovascular care - leading to better patient outcomes, improved quality of care, and reduced healthcare costs. Come work at Elucid and be part of delivering on our mission to prevent heart attacks and strokes!
Every product we build has to earn its way to patient care, and regulatory strategy is how it gets there. We're looking for a Director of Regulatory who thrives on translating complex, evolving global requirements into clear paths to clearance for AI-enabled medical imaging software. You'll lead the execution of our regulatory strategy across FDA, EU MDR and other international markets, guiding submissions from pre-sub through post-market lifecycle management for a quickly growing startup. Partnering closely with our Quality, Engineering, Clinical, Commercial and Product teams, you'll sit at the center of how we bring innovative cardiovascular software safely and compliantly to the people who need it.
The ideal candidate will have:
  • 7+ years of Regulatory Affairs experience in the medical device industry, with a track record of successful submissions in the US and EU (pre-submissions, IDEs, 510(k)s, De Novo, EU MDR product registrations).
  • Advanced degree in Regulatory Affairs, Life Sciences, Engineering, or a software-related discipline.
  • 2-5+ years of people management experience, with strong cross-functional collaboration and communication skills.
  • Expertise in global device regulatory requirements and standards (21 CFR Part 820, EU MDR, ISO 13485, ISO 14971, IEC 62304, IEC 62366). Experience in Software as a Medical Device (SaMD); familiarity with FDA Class II devices and EU MDR Class IIa/IIb products preferred.
  • Strong collaboration and communication skills, with the ability to translate complex regulatory requirements into actionable guidance and drive effective, cross-functional execution.
Work Location:
  • This role is based out of our office in Boston, MA. For local candidates, we operate in a hybrid model with regular in-office collaboration. Candidates outside of the Boston area are invited to apply as fully-remote employees.
Salary Range:
  • The anticipated base salary range for this position at Elucid is $175,000-$225,000. Compensation will be influenced by a wide array of factors including but not limited to internal pay equity, job-related knowledge, skills, education, relevant experience, certifications, and geography as outlined in the job description.
HQ

Elucid Boston, Massachusetts, USA Office

2 Park Plaza, 700, Boston, MA, United States, 02116

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