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Provide Medical Safety/PV inputs to the assigned products at Jazz Pharmaceuticals, which may include Clinical Development program of all phases, Investigator Sponsored, Compassionate Use, and Disease Monitoring Programs; liaise with Clinical Sciences, Clinical Operations, Medical Affairs, Biometri
Minimum 2-5 years of Clinical Development, Medical Affairs or Drug Safety/Pharmacovigilance experience; other relevant medical affairs experience may be considered. The Global Safety Physician serves as the safety expert accountable for the global safety strategy and overall safety profile for Jazz
Excellent writing and editorial skills, ability to collaborate on development of high‑quality clinical‑regulatory documents, eg, investigator brochures, meeting request/package. Lead to deliver high quality and timely regulatory submissions in alignment with corporate goals, and in compliance wi
ORIC Pharmaceuticals is seeking a Director/Associate Director in Regulatory Affairs to support clinical development of oncology products. This role requires at least 8 years of regulatory affairs experience and excellent communication skills. The successful candidate will support regulatory submissi
Associate Director, Development Quality Assurance. A bachelor’s degree with a minimum of 12 years of GCP quality assurance experience, a master’s degree with a minimum of 8 years of relevant experience, a PhD with a minimum of 5 years of relevant experience, or an equivalent combination of educa
Serve as the signatory and overseer of the preparation and review of pre- and postmarketing aggregate safety reports including Periodic Safety Update Reports (PSURs)/Periodic Benefit Risk Evaluation Reports (PBRERs), Periodic Adverse Drug Experience Reports (PADERs), Development Safety Update Report
Serve as the signatory and overseer of the preparation and review of pre- and postmarketing aggregate safety reports including Periodic Safety Update Reports (PSURs)/Periodic Benefit Risk Evaluation Reports (PBRERs), Periodic Adverse Drug Experience Reports (PADERs), Development Safety Update Report
Manager- Professional Development/Patient Safety/Magnet - Sharp Coronado Hospital - FT - DaysSkip to main content#Manager- Professional Development/Patient Safety/Magnet - Sharp Coronado Hospital - FT - Days page is loaded## Manager- Professional Development/Patient Safety/Magnet - Sharp Coronado Ho
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. Minimum of 8 years of regu
Sharp HealthCare in San Diego, California, seeks a Registered Nurse (RN) to provide nursing services to patients and families. Candidates will engage in diverse responsibilities, including patient education and care coordination, within a supportive team environment.
Manager, Trial Disclosure, Medical Writing Operations page is loaded## Manager, Trial Disclosure, Medical Writing Operationsremote type:. Position Summary:**The Manager of Medical Writing Operations - Trial Disclosure role is responsible for clinical trial transparency and disclosure activities, inc
This role focuses on regulatory strategy execution for drug development. A biopharmaceutical company in San Diego seeks an Associate Director, Regulatory Affairs CMC. The ideal candidate has 10 years of experience in Regulatory Affairs within the biopharmaceutical industry, including supervisory rol
A leading pharmaceutical company is seeking a Senior Medical Affairs Operations Manager to oversee the execution of clinical studies and manage the medical affairs operation. The role requires managing clinical protocols, leading teams, and ensuring compliance with regulatory standards.
Retina Consultants San Diego is the oldest and most prestigious Retina practice in San Diego, with concierge-level patient care, high standards for professionalism and quality, advanced imaging modalities, heavy involvement in cutting-edge clinical trials, and exposure to advanced medical and surgic
Minimum 2-5 years of Clinical Development, Medical Affairs or Drug Safety/Pharmacovigilance experience; other relevant medical affairs experience may be considered. The Global Safety Physician serves as the safety expert accountable for the global safety strategy and overall safety profile for Jazz