On Site Jobs in California
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Director, Patient Marketing
Director, Patient Marketing Location: San Francisco, CA - 3 days on site EPM Scientific is partnered with a rapidly growing biotechnology organization dedicated to developing transformative treatments for individuals living with serious and underserved conditions, particularly within rare and genetically driven diseases. Built on a model that empow...
Associate Director Clinical Operations
Minimum QualificationsBachelor's degree in a scientific or life sciences discipline~10+ years of relevant experience within clinical operationsRequired Experience & CapabilitiesDirect experience supporting or leading clinical studies in acute and/or chronic pain, with meaningful exposure to study execution challenges in this spaceStrong working kno...
Senior Scientist, LC-MS
Job TitleSenior Scientist or Associate Principal Scientist, LC-MS PlatformsPosition SummaryA San Francisco based contract research organization (CRO) delivering globally recognized GLP/GCLP-compliant bioanalytical and biomarker services. We partner with multinational pharmaceutical and biotechnology companies to support their drug development progr...
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Director, Patient Marketing Neurology
Director, Patient Marketing (Neurology) Location: San Francisco, CA - 3 days on site EPM Scientific is partnered with a rapidly growing biotechnology organization dedicated to developing transformative treatments for individuals living with serious and underserved conditions, particularly within rare and genetically driven diseases. Built on a mode...
Regulatory Affairs Lead
Regulatory Affairs LeadPosition Summary The Regulatory Affairs Lead will provide strategic and operational regulatory support across the product lifecycle for Class III medical devices. This role will partner cross‑functionally to help ensure regulatory alignment, support global submissions, and maintain compliance with applicable regulations.Key ...
Regulatory Affairs Lead
Regulatory Affairs LeadPosition Summary The Regulatory Affairs Lead will provide strategic and operational regulatory support across the product lifecycle for Class III medical devices. This role will partner cross‑functionally to help ensure regulatory alignment, support global submissions, and maintain compliance with applicable regulations.Key R...
