As part of our NovoFlex hybrid policy, this role requires in-office presence in Portsmouth, NH at least three times per week.

Novocure is pioneering cancer treatment through Tumor Treating Fields (TTFields) and is seeking a Medical Review Specialist to join our Post-Market Safety team based in Portsmouth, NH. In this role, you’ll assess adverse event reports, ensure accurate medical coding, and support global regulatory compliance for our medical devices.

Key Responsibilities:
• Review medical case narratives and adverse event complaints
• Ensure accurate MedDRA coding and data completeness
• Evaluate case reportability under global regulations
• Identify safety signals and support aggregate reporting
• Provide guidance on coding and compliance

What You Bring:
• PharmD, RN, or healthcare-related degree
• 2+ years in pharmacovigilance, product safety, or related field
• Familiarity with US medical records, MedDRA, and complaint systems
• High attention to detail and ability to work independently
• Strong communication skills and a team-first mindset

Join Novocure and help redefine what’s possible in cancer treatment. We are an Equal Opportunity Employer, including Veterans/Disabled.