Fda Regulations Jobs in San Francisco, CA

We are seeking a highly experienced Principal Research Scientist II to lead and oversee toxicology and safety pharmacology studies as well as preclinical safety strategy for compounds under development at AbbVie. In this role you will provide strategic input for toxicology safety asse More...

The Senior Associate Counsel Clinical Trials and Research provides legal support for clinical trial and research activities across the University of Maryland Medical System (UMMS). This role involves refining processes to streamline timetoactivation for clinical trials standardizing c More...

The Thought Leader Liaison (TLL) is a fieldbased marketing professional responsible for collaborating with internal teams and external stakeholders. A successful TLL fosters effective bidirectional communication between customers and the organizations internal ecosystem supports curre More...

Description: Must meet all requirements for Clinical Project Assistant position and have demonstrated proficiency in all relevant areas. Provides administrative assistance in site selection study implementation and ongoing coordination of study sites either directly or via CROs. Moni More...

The Manager Global Regulatory Strategy US & Canada is responsible for the development and implementation of US and Canada regulatory strategic and tactical planning (RSTP) for assigned on market products or those products in development. This individual assists Regulatory Staff by More...

Resource Management and Training:Participation in QM resource allocationResource allocation of QA auditorsFacilitation of professional development and career advancement of Quality Management staffAdministrative supervision of Quality Management staff jointly with Senior Director Qual More...

Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients worldwide. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The com More...

Description: Job Title: Clinical Trials Management Associate II Location: Foster City CA Duration: 06 months with possible extension Shift Details: 1st shift/ Monday Friday 8am5pm/business hours Essential Duties and Responsibilities Leads or manage components of Phase I II More...

Job Title: Manager/Sr Manger/Associate Director Regulatory Affairs (Strategy Hematology Job Location: San Francisco Bay Area CA USA Job Location Type: Remote Job Contract Type: Fulltime Job Seniority Level: MidSenior level Nurix Therapeutics is a clinical stage biopharmaceutical comp More...

Job Title: Clinical Document Manager Job Location: San Francisco CA USA Job Location Type: Remote Job Contract Type: Contract Job Seniority Level: MidSenior level OverviewWe are currently searching for a skilled professional to join a wellknown client’s team as a Clinical Docu More...

About This Role The Senior Manager GCP Quality Assurance & Governance in R&D Quality and Compliance provides global strategic leadership for quality and oversight of quality activities in Biogen R&Ds ongoing clinical research and development processes and programs partneri More...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.HomeBased in the United StatesResponsibilities:Advise clients project teams sites data safety monitoring boards More...

Job Title Validation Process Monitoring and Data Analytics Engineer Location Parsippany NJ Hybrid Onsite T/W/Th Working hours: 84:30 8:305 95:30 type of hours (most of team works 95) Job Duration: 12 months Responsibilities: Strong background in statistics process monitori More...

Regional Overview and Travel Requirements:Must reside in:  San Francisco Bay Area or surrounding regionsRegion covers but not limited to:  Northern CaliforniaTravel:  80% including overnightsReports to:  Regional Service ManagerPosition Summary:At Cutera we know th More...

About This Role The Associate Director Statistical Programming will be reporting to the Statistical Programming & Clinical Data Sciences Lead for Biogens West Coast Hub. He/She will lead and oversee statistical programming activities of internally and externally through vendors en More...

Essential Job ResponsibilitiesThe FSE performs the major functions listed below. The position may require additional duties/responsibilities that may not be outlined below and specific functions are subject to change. Analyzes troubleshoots and repairs diagnostic and/or other imaging More...

Manage and oversee all aspects of state and local income tax operations including reporting compliance planning and auditsLead the preparation of state and local income tax provision and collaborate with the tax provision teams to ensure alignment and compliance with overall tax strat More...

Manage and oversee all aspects of state and local income tax operations including reporting compliance planning and auditsLead the preparation of state and local income tax provision and collaborate with the tax provision teams to ensure alignment and compliance with overall tax strat More...

destinationone Consulting specializes in recruitment across diverse sectors including CleanTech Education and EdTech Government (Municipal State/Provincial and Federal) Health and MedTech Healthcare and Wellness Legal NotForProfit and Public Accounting. We are committed to building a More...

Your CareerThe Supply Chain Compliance Manager will drive compliance  programs within the supply chain focusing on ensuring our products meet regulatory requirements.  This role includes staying current with global regulations conducting gap assessments and ensuring complian More...