Additionally, 5 years of experience in pharmacy benefit management and managed care health plan working with large pharmacy and medical claims data sets is required. The Pharmacy Markets, Products, Analytics and Strategies (RxMAPS) team is responsible for leading and collaborating cross-functionally
The position provides direct patient care that regularly involves heavy lifting and moving of patients and assisting with ambulation. Fresenius Medical Care maintains a drug-free workplace in accordance with applicable federal and state laws. Assists in training of applicable direct patient care sta
Partner with Medical Writing, Regulatory Operations, Clinical Development, Biometrics, Pharmacovigilance, and other functions to ensure documents are submission-ready and comply with regulatory publishing requirements. The Manager, Medical Writing Operations is responsible for leading document speci
Experience working as a medical assistant as a patient care coordinator. Scheduling new patient's appointments, registration of any new patient, mailing of New Patient Paperwork as needed. Retina Consultants San Diego is the oldest and most prestigious Retina practice in San Diego, with concierge-le
Leads the development and oversight of the processes and procedures relevant to the creation, review and approval of advertising and promotional materials as part of Acadia Medical, Legal and Regulatory review process and other external communication to ensure regulatory compliance. This role overse
What You Will Do The Senior SpecialistPerformance Improvement-Licensing and Accreditation is responsible for the development and implementation of performance improvement standards with a primary emphasis on regulatory affairs, licensing, accreditation, risk management, patient safety, and adverse e
Ortho Clinical Diagnostics is seeking a Systems Engineer II to support point-of-care medical devices in San Diego, CA. The role involves hands-on experience in system design, analysis, and integration, ensuring alignment with regulatory standards.
The Associate Director, Regulatory Affairs Project Planning & Coordination is responsible for developing, implementing, and monitoring project plans and best practices that facilitate how the Global Regulatory Affairs department executes its strategic and functional goals. Partner with R&D initiativ
Typically 8+ years of relevant experience in Medical Affairs, pharmaceutical or biotechnology operations, commercial operations, clinical operations, or related healthcare industry functions. The Manager, Medical Affairs Operations provides strategic and operational leadership for the Medical Affair
The Senior Director, Regulatory Operations provides strategic and operational leadership for global regulatory operations, overseeing electronic submissions, regulatory information management systems, and end-to-end submission execution. Minimum of 12 years of progressively responsible experience in