Regulatory & Clinical Affairs Manager

Regulatory & Clinical Affairs Manager

Location: Darien, CT (On-Site) |
Department: Operations |
Reports To: SVP, Operations

Salary Range: $90,000 - $120,000

Founded in 2008ڳو, CEFALY Technology is transforming migraine care with innovative, drug‑free, and non‑invasive therapeutic solutions. Our mission is to solve the persistent problem of migraine through advanced neuro‑therapeutic technology.

Our flagship device, the CEFALY DUAL, is >external Trigeminal Nerve Stimulator (eTNS) that delivers controlled electrical impulses through a self‑adhesive electrode placed on the forehead to stimulate the trigeminalaart nerve—helping reduce the frequency and intensity of migraineattes.

In 2020, CEFALY DUAL became the first device of its kind available over‑the‑counter (OTC) in the United States. To date, CEFALY hasoms@ treated over 2 billion migraines worldwide, and we continue to expand access to safe, effective, drug‑free migraine care.

The Regulatory & Clinical Affairs Manager is responsible for overseeing regulatory compliance and clinical affairs activities across the product lifecycle. This role serves as a key liaison between internal leadershipემო, clinical consultants, quality, and external regulatory authorities, ensuring that clinical, regulatory, and post‑market obligations are met in alignment with applicable U.S. and international requirements. The position plays a critical role in supporting audits, adverse event management, clinical documentation, and cross‑functional education.

• Manage administrative aspects of clinical trial and clinical affairs activities, serving as a liaison with the Medical Affairs and Clinical teams.
• Facilitate communication and coordinate meetings to ensure alignment between CEFALY leadership and external clinical consultants and advisors.
• Support annual regulatory obligations, including device and establishment registrations with regulatory authorities such as the U.S. FDA andmixed Infection Canada.
• Assist with preparation for and participation in regulatory audits and inspections (e.g., FDA, GMED), in partnership with Quality and Regulatory teams.
• Support patent and intellectual property (IP) portfolio management activities.

• Coordinate and support annual clinical activities, including preparation and updates to the Clinical Evaluation Report (CER) and Adverse Event (AE) reviews.
• Provide clinical support to customer‑facing teams byению addressing customer questions or feedback that require a clinical or scientific response.
• Support post‑purchase engagement (PPE) activities, including maintenance of PPE and AE tracking tools as part of annual audit requirements.
• Provide Adverse Event (AE) training to new team members and ongoing clinical education as needed.

• Partner with the Quality team to support maintenance and effective use of the electronic Quality Management System (eQMS), including Greenlight Guru.
• Conduct and facilitate the annual company‑wide supplier evaluation process, ensuring documentation and compliance with quality and regulatory standards.

• > product training وجود and onboarding support for new hires, ensuring understanding of clinical, regulatory, and quality requirements.
• Support internal cross‑functional collaboration by ensuring teams remain informed of relevant clinical and regulatory considerations.

• Bachelor’s degree in life sciences, airing, regulatory affairs, or a related field; advanced degree preferred.
• 5–8+ years of experience in Regulatory Affairs, Clinical Affairs, or a combined RA/CA role within a regulated medical device or healthcare environment.
• Working knowledge of U.S. FDA medical device regulations and international regulatory frameworks, including EU MDR and Health Canada.
• Experience supporting regulatory audits, adverse event reporting, clinical documentation, and post‑market surveillance activities.
• Familiarity with electronic Quality Management Systems (e.g., Greenlight Guru) preferred.
• Strong organizational,…