Director, Downstream Process Development Allakos Therapeutic antibodies Mast cells and EosinophilsDirector, Downstream Process DevelopmentRedwood City, CaliforniaThis position leads the Purification Group which is responsible for the process development, tech transfer, supervision of Engineering and Clinical batches, BLA enabling activities, PPQ Batches and commercial production at multiple CMO sites, process characterization and BLA authoring and review. Position Summary: The Director, Downstream Process Development would be key member of Biologics DS development and tech transfer team and would be responsible for all activities related to Downstream Process Development of our late-stage clinical biologics (Mab) molecule AK002 and early stage program.
Director, Corporate Counsel, Early Research & Development BioMarin Pharmaceutical IncDirector, Corporate Counsel, Early Research & DevelopmentSan Rafael, CA$204,000–$280,500 / yearThe successful candidate will possess deep experience negotiating and drafting complex research and collaboration agreements including licenses, strong intellectual property acumen, and a demonstrated ability to effectively partner with scientists and senior business leaders in a fast-paced life sciences environment. Our revolutionary treatments for conditions like achondroplasia (the most common form of dwarfism), PKU (phenylketonuria), CLN2, a form of Batten disease, and a number of forms of MPS (mucopolysaccharidosis) offer new possibilities for patients and families who previously had few, if any, available options.
Director, CMC Regulatory Corvus PharmaceuticalDirector, CMC RegulatorySAN FRANCISCO, CAFull timeReporting to the Vice President of Regulatory Affairs, the Director of Regulatory Affairs CMC will serve as a key member of the Regulatory organization, responsible for developing and executing global Chemistry, Manufacturi ng, and Controls (CMC) regulatory strategies for clinical-stage small molecule programs. This individual will partner cross-functionally with CMC, Technical Operations, Quality, and Clinical teams to ensure timely, compliant, and high-quality regulatory submissions and lifecycle management activities.
Executive Director Fremont and Fostoria ProMedicaExecutive Director Fremont and FostoriaFremont, CaliforniaBachelor’s Degree in relevant field of study and three years or more experience in a sophisticated development, customer service, sales, business role; healthcare-related preferred. It serves communities across nine states and provides a range of services, including acute and ambulatory care, a dental plan, and academic business lines.
Senior Manager, Clinical Business Systems Structure Therapeutics IncSenior Manager, Clinical Business SystemsSouth San Francisco, CA$166,000–$209,000 / yearReporting to the Associate Director, GxP Operations, this role is the primary operational owner and business partner for validated platforms supporting Clinical, Quality, Regulatory, and Technical Operations, including Veeva Vault QMS, QualityDocs, LMS, CTMS, and eTMF; Box; DocuSign; and other regulated systems. The company's platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs.
Sr. Pharmacovigilance (PV) Clinical Scientist LancesoftSr. Pharmacovigilance (PV) Clinical ScientistSouth San Francisco, CA$66.13PV Clinical Scientist leads clinical review of US Government Client cases (processed in-house or externally by the vendor) and supports the US Patient Safety PV Clinical Associate Group Director and PV Clinical Group Director-PV Compliance Team in all activities. Acts as single point of contact with key stakeholders for safety-related activities, identifies potential business gaps, and assists in the development and implementation of process solutions, and leads projects as assigned and under the direction of the US Patient Safety PV Clinical management.
Non-Clinical - Radiology Didactic Trainer 22nd Century Technologies, Inc.Non-Clinical - Radiology Didactic TrainerSan Francisco, CAThe program is organized across six consecutive 11-week terms (approximately 25 28 contact hours per week) and integrates asynchronous online coursework, weekly online meetings with instructors, face-to-face laboratory sessions, and supervised clinical rotations at five UCSF-affiliated imaging sites (UCSF Parnassus, Mission Bay, Mt. The UCSF Radiologic Technologist Training & Leadership Academy is an 18-month, full-time entry-level radiography program, developed in partnership with City College of San Francisco (CCSF) and designed to prepare students for competent, compassionate entry-level practice as radiologic technologists.
Non-Clinical - Radiography Orientation Instructor 22nd Century Technologies, Inc.Non-Clinical - Radiography Orientation InstructorSan Francisco, CAThe program is organized across six consecutive 11-week terms (approximately 25 28 contact hours per week) and integrates asynchronous online coursework, weekly online meetings with instructors, face-to-face laboratory sessions, and supervised clinical rotations at five UCSF-affiliated imaging sites (UCSF Parnassus, Mission Bay, Mt. The UCSF Radiologic Technologist Training & Leadership Academy is an 18-month, full-time entry-level radiography program, developed in partnership with City College of San Francisco (CCSF) and designed to prepare students for competent, compassionate entry-level practice as radiologic technologists.
Clinical Effectiveness Consultant, CV Services Sutter HealthClinical Effectiveness Consultant, CV ServicesSan Francisco, CA$99.88–$139.82 / hourEmployees of Sutter Health and its entities may handle hazardous drugs in the course of their work, including patient care, which requires them to manage, store, prepare, receive, unpack, transport, dispose of, or administer drugs identified as hazardous or potentially hazardous by the National Institute for Occupational Safety and Health (NIOSH) and in accordance with the USP 800 guidelines. Leads and facilitates the development, deployment, and monitoring of clinical quality improvement projects, patient safety improvement initiatives, and organization improvements to achieve top decile clinical outcomes and accelerate the achievement of clinical quality and safety goals.
Sr. Clinical Research Associate Structure Therapeutics IncSr. Clinical Research AssociateSouth San Francisco, CA$135,000–$145,000 / yearOverall management of selected clinical sites including acting as a point of escalation and oversight of CRO monitoring activities, which includes monitoring visit report review, contract and budget negotiations with clinical sites. The company's platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs.
Sr. Clinical Research Associate/Clinical Trial Manager BridgeBio Pharma IncSr. Clinical Research Associate/Clinical Trial ManagerSan Francisco, CA$135,000–$177,000 / yearLead aspects of vendor management for the CRO and other key vendors (IRT, imaging, central and specialty labs, etc.), establishing expectations, ensuring deliverables are met, performance measures are maintained, and escalating as needed; address performance gaps and drive corrective actions to closure. Lead operational management for assigned regions and sites by monitoring performance metrics, identifying and mitigating risks, driving escalations and action-item closure, and representing regional performance in study team and cross-functional discussions.
Clinical Effectiveness Consultant IV Sutter HealthClinical Effectiveness Consultant IVEmeryville, CA$62.11–$93.17 / hourLeads and facilitates the development, deployment, and monitoring of clinical quality improvement projects, patient safety improvement initiatives, and organization improvements to achieve top decile clinical outcomes and accelerate the achievement of clinical quality and safety goals. Assigned to specific performance improvement teams, to provide clinical expertise, performance improvement consultation, analysis, gap assessment, group/team facilitation and development, and guidance for the dissemination of practices that result in improved clinical outcomes.
NewSenior Pharmacovigilance (PV) Clinical Scientist Iconma LLCSenior Pharmacovigilance (PV) Clinical ScientistSouth San Francisco, CAActs as single point of contact with key stakeholders for safety-related activities, identifies potential business gaps, and assists in the development and implementation of process solutions, and leads projects as assigned and under the direction of the US Patient Safety PV Clinical management. PV Clinical Scientist leads clinical review of USPS cases (processed in-house or externally by the vendor) and supports the US Patient Safety PV Clinical Associate Group Director and PV Clinical Group Director-PV Compliance Team in all activities.
NewClinical Operations Liaison (Full-Time, Remote) Sprinter HealthClinical Operations Liaison (Full-Time, Remote)Menlo Park, CaliforniaRemote$65,000–$75,000 / yearYou’ll be the connective thread between our NPs and Sprinters (our clinician field staff) and the operational systems that keep them paid, trained, and compliant — handling workforce tracking, payroll compliance follow-up, documentation review, and reporting so clinical leadership can stay focused on patient care, clinical support, and clinical oversight. At Sprinter Health, our mission is to dramatically expand access to healthcare by reimagining the patient experience—delivered at home and powered by technology for scale.
NewClinical Operations Liaison (Full-Time, Temporary) $1k Bonus Sprinter HealthClinical Operations Liaison (Full-Time, Temporary) $1k BonusMenlo Park, California$65,000–$75,000 / yearYou’ll be the connective thread between our NPs and Sprinters (our clinician field staff) and the operational systems that keep them paid, trained, and compliant — handling workforce tracking, payroll compliance follow-up, documentation review, and reporting so clinical leadership can stay focused on patient care, clinical support, and clinical oversight. At Sprinter Health, our mission is to dramatically expand access to healthcare by reimagining the patient experience—delivered at home and powered by technology for scale.
NewSenior Pharmacovigilance (PV) Clinical Scientist IconmaSenior Pharmacovigilance (PV) Clinical ScientistSouth San Francisco, CA$50.76–$69.85 / hourActs as single point of contact with key stakeholders for safety-related activities, identifies potential business gaps, and assists in the development and implementation of process solutions, and leads projects as assigned and under the direction of the US Patient Safety PV Clinical management. PV Clinical Scientist leads clinical review of USPS cases (processed in-house or externally by the vendor) and supports the US Patient Safety PV Clinical Associate Group Director and PV Clinical Group Director-PV Compliance Team in all activities.
Hospice Clinical Manager (RN) Sequoia Home Health and HospiceHospice Clinical Manager (RN)Concord, CaliforniaThe Pennant Group, Inc. is a holding company of independent operating subsidiaries that provide healthcare services through home health and hospice agencies and senior living communities located throughout the US. This role ensures clinical excellence, supervises interdisciplinary team members, and supports clinicians in providing outstanding patient-centered care.
Medical Director, Clinical Research Cardiovascular Cytokinetics, IncorporatedMedical Director, Clinical Research CardiovascularSouth San Francisco, CA$276,120–$322,140 / yearCytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction. The individual will also partner with members of the new product planning group to assist with market research, defining the target product profile, and health economics and outcomes research, as well as serving as a consultant to evaluate new projects in research and outside licensing opportunities.
Medical Director, Clinical Research Neuromuscular Cytokinetics, IncorporatedMedical Director, Clinical Research NeuromuscularSouth San Francisco, CA$276,120–$322,140 / yearMD or MD/PhD degree with internal medicine or neurology board certification by the American Board of Internal Medicine with a minimum of 2+ years of experience in clinical development, either in a biotechnology or pharmaceutical company or as a clinical investigator, including industry-sponsored multi-center trials. Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction.
Director, Compute Infrastructure Procurement Operations AnthropicDirector, Compute Infrastructure Procurement OperationsSan Francisco, CA$300,000–$385,000 / yearYou will simultaneously operationalize three enterprise-scale initiatives: a multi-entity procurement structure spanning domestic and international jurisdictions, a compliance-critical Asset Lifecycle Management program and procurement operations for Anthropic data center sites across the US with international expansion underway. Anthropic is seeking a Director of Compute Infrastructure Procurement Operations to build and lead the function responsible for how Anthropic procures, tracks, and governs its compute infrastructure assets at scale.