Part of Phaidon International![]()
Showing 26 results
Sort by:
Government Programs & Provider Support Specialist San Mateo, CA (Hybrid: 3 days onsite, 2 days remote)An innovative global specialty pharmaceutical company is seeking a Government Programs & Provider Support Specialist to join its North American Operations team. This individual will serve as a key resource for providers, specialty centers, patients...
Government Programs & Provider Support SpecialistSan Mateo, CA (Hybrid: 3 days onsite, 2 days remote)An innovative global specialty pharmaceutical company is seeking a Government Programs & Provider Support Specialist to join its North American Operations team. This individual will serve as a key resource for providers, specialty centers, patients,...
Head of Regulatory AffairsLocation: Boston, MA (Hybrid) Company: Growth-Stage AI/ML Diagnostics & Digital Health Company Company Size: 200-500 EmployeesAbout the CompanyWe are a rapidly growing healthcare technology company developing innovative AI/ML-enabled diagnostic and Software as a Medical Device (SaMD) solutions that empower clinicians with...
Take the first step toward your next opportunity - submit your resume and get started today.

Director / Senior Director, Regulatory Strategy Clinical-stage biotech | San Francisco Bay Area | HybridWe're partnering with an innovative clinical-stage biotech that is advancing novel biologic therapies in areas of high unmet need. As the pipeline progresses through the clinic, the company is looking for a strategic, hands-on regulatory leader t...
EPM Scientific are working alongside a global biopharmaceutical company that is seeking a Head of Global Regulatory Strategy to lead regulatory strategy for a high-profile injectable aesthetics portfolio. This individual will provide strategic leadership across both biologic and medical device products, with primary responsibility for neurotoxin pr...
Position SummaryThe Principal R&D Engineer provides technical leadership for the development, verification, validation, and commercialization of Class II and Class III medical devices. This individual serves as a subject matter expert responsible for driving complex product development programs from concept through design transfer while ensuring co...