NewCrisis Clinical Program Manager Pacific ClinicsCrisis Clinical Program ManagerSan Jose, California$106,022–$130,394 / yearMaster's Degree (M.A) degree in Social Work or a closely related field (e.g., Marriage, Child and Family Counseling or Psychology) and four (4) or more years of clinical experience with children, or adults, including crisis management experience, or equivalent combination of education and experience (two years of relevant experience equals one year of education) to include: Two (2) years of supervised clinical experience with children and or adults. This position will require at times providing back up to the Clinician positions in which will jointly respond with law enforcement officers, participating in crisis assessment and triage including the screening for dangerous situations, weapons and other high risk environmental factors, responsible for crisis de-escalation and stabilization in situations that have the potential for becoming volatile in nature and assisting with transporting/transitioning individuals to the lowest level of care.
Head of Clinical Science Convergent ResearchHead of Clinical ScienceSan Francisco, CAFull timeNice to have: experience with focused ultrasound, functional ultrasound, DBS, or TMS; transdiagnostic and dimensional approaches to psychiatric symptoms; work with large multimodal imaging datasets; IRB and regulatory experience. We're looking for someone to lead how Arbor approaches applied human neuroscience and how we think about clinical impact: which conditions we work on, which symptoms we try to move, and what it would mean to succeed.
vIOP Clinical Quality Manager Lyra Health IncvIOP Clinical Quality ManagerCA$136,800–$152,000 / yearThis role is a great fit if you have training, experience, and expertise in treating clients (young adults and adolescents) with mood and anxiety disorders in an intensive outpatient program setting, as well as a commitment to evidence-based and culturally responsive care, clinical quality assurance, experience in administrative and clinical management of licensed independent mental health providers and case managers, and developing high performing teams. We are looking for an experienced mental health clinical leader with a passion for clinical quality and management to serve as a clinical quality manager and lead for our Pediatric virtual Intensive Outpatient Program (vIOP), an accelerated, comprehensive care experience that helps young people ages 7 to 25 feel better quickly from the comfort of home.
Executive Director, GCP QA (Good Clinical Practice, Quality Assurance) Revolution Medicines, Inc.Executive Director, GCP QA (Good Clinical Practice, Quality Assurance)Redwood City, CA$265,000–$331,000 / yearMinimum of 15 years of experience in the pharmaceutical or biotechnology industry, including at least 10 years in GCP QA or clinical quality leadership roles, with demonstrated experience leading and hosting regulatory inspections (e.g., FDA BIMO, EMA, MHRA, PMDA). Serving as the GCP QA lead for late-stage clinical programs, this individual is accountable for GCP, GLP, and Pharmacovigilance/Safety oversight across multiple RevMed studies and represents QA in cross-functional and executive forums.
Vice President, Translational Medicine & Clinical Pharmacology Rigel Pharmaceuticals, Inc.Vice President, Translational Medicine & Clinical PharmacologySouth San Francisco, CA$306,000–$365,000 / yearLead clinical pharmacology strategy and development plans for Rigel assets, including ADME, drug-drug interactions (DDIs), pharmacokinetics/pharmacodynamics (PK/PD), exposure-response, bioavailability/bioequivalence, and other studies required to characterize dose, regimen, safety, and efficacy. Advanced scientific degree (PhD, PharmD, MD, or equivalent) in pharmacology, pharmaceutical sciences, drug metabolism, toxicology, translational medicine, or a related discipline; PhD or PharmD strongly preferred for a clinical pharmacology-focused role.
Clinical Lab Scientist Supervisor UCSF Medical CenterClinical Lab Scientist SupervisorSan Francisco, CAPerform quality management activities, which may include, but are not limited to, completion of monthly QA reports; monitoring and analysis of quality control results and L-J plots; ensuring all required maintenance are properly performed and documented; timely monitoring and completion of employee competency requirements; assessment of proficiency test results; actively investigates and ensures proper documentation of corrective action and resolution involving failures and errors in proficiency testing, patient testing, inspections, instrumentation, method validations and processes. Under the general direction of the Core Lab Manager, the incumbent will supervise Clinical Laboratory Scientists, Clinical Laboratory Scientist Specialists, and Hospital Laboratory Technicians in the Core Lab; collaborate and coordinate with various divisions of the Clinical Laboratory and with all related services at ZSFG, affiliated hospitals, health centers, clinics, and outreach clients.
Licensed Clinical Program Manager, (LCSW/LMFT Required) San Mateo FSP Bay Area Community ServicesLicensed Clinical Program Manager, (LCSW/LMFT Required) San Mateo FSPSan Mateo, CAThe Program Manager is responsible for leading an ACT (Assertive Community Treatment) team providing direct service to acute mental health crisis cases in our new Full Service Partnership (FSP) Program in San Mateo. Bay Area Community Services is a CARF accredited non-profit, community-based agency celebrating over 70 years of serving Alameda, Contra Costa,Sacramento and Solano Counties by providing mental health and social services.
Sr. Manager, Clinical Data Management Shifamed LLCSr. Manager, Clinical Data ManagementLos Gatos, CA$150,000–$180,000 / yearThe role ensures data is captured completely, accurately, and in a state that is audit-ready and submission-ready, and works cross-functionally with Biostatistics, Clinical Operations, Monitoring, Medical Safety, and Regulatory Affairs to keep the trial''s data infrastructure aligned to study needs from first-patient-in through database lock. This individual translates the protocol and statistical analysis plan into a data capture strategy that is fit for purpose, then partners closely, day to day, with a Data Manager to build, validate, and maintain the EDC and related clinical systems (randomization/IWRS, imaging, safety, and patient screening databases) against that strategy.
Clinical Product Expert Profound Medical IncClinical Product ExpertSan Francisco, CAGeneral Accountability TULSA-PRO clinical product experts support the widespread adoption and utilization of the TULSA Procedure by educating, mentoring, and collaborating with urologists, radiologists, and their staff on the technical and clinical aspects of MRI-guided transurethral ultrasound ablation of the prostate using Profound Medicals TULSA-PRO system. Perform detailed post-treatment case reviews, including analyses of treatment workflow and patient outcomes for the sites they support, identifying rate-limiting steps and areas for improvement to coach physicians and their teams towards more efficient procedures and optimal patient outcomes across a wide variety of prostate disease states.
MR Clinical Excellence Leader - Academic - Greater San Francisco Area GE HealthCare Technologies IncMR Clinical Excellence Leader - Academic - Greater San Francisco AreaSan Francisco, CA$156,000–$234,000 / yearPartner with the SBU (Strategic Business Unit) and Modality teams to provide insights of customer learnings and competition; provide a feedback loop to SBU and Modality teams on product performance at assigned academic sites. Establish and drive relations, collaboration, and partnerships with all department/relevant stakeholders; engage with key opinion leaders on progress made and gain consensus on next steps/actions.
Clinical Trial Assistant Revolution Medicines, Inc.Clinical Trial AssistantRedwood City, CA$90,000–$108,000 / yearThe Clinical Trial Assistant of Clinical Operations, initially reporting to the Director, Clinical Operations, will be responsible for acting as a central contact for the clinical study teams and assist with the clinical execution and management to support RevMed clinical trials. Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS.
Associate Director, Clinical Operations Structure Therapeutics IncAssociate Director, Clinical OperationsSouth San Francisco, CA$186,000–$220,000 / yearCross-Functional Collaboration: Work closely with Preclinical, Biostatistics, Data Management, Clinical Supplies, Safety/PV, and Medical Affairs teams to ensure seamless study execution and IMP accountability, including sample management and study plan reviews. 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.
Associate Director, Clinical Operations (SF Bay Area) Structure Therapeutics IncAssociate Director, Clinical Operations (SF Bay Area)South San Francisco, CA$186,000–$220,000 / yearCross-Functional Collaboration: Work closely with Preclinical, Biostatistics, Data Management, Clinical Supplies, Safety/PV, and Medical Affairs teams to ensure seamless study execution and IMP accountability, including sample management and study plan reviews. 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.
Senior Scientist I, Cancer Genomics, Clinical Biomarker Development Revolution Medicines, Inc.Senior Scientist I, Cancer Genomics, Clinical Biomarker DevelopmentRedwood City, CA$149,000–$186,000 / yearExperienced in the interrogation of DNA sequence data derived from tumor tissue, such as gene-panel, whole-exome or whole-genome data and downstream analytics (clonality estimates, copy number variation, chromosomal instability, mutational signatures, etc). Leveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS.
Clinical Product Manager (PhD/PsyD) Lyra Health IncClinical Product Manager (PhD/PsyD)CA$106,000–$162,500 / yearOutside of the United States, for example in the EU, Switzerland and the UK, you may have the right to request access to, or a copy of, your personal information, including in a portable format; request that we delete your information from our systems; object to or restrict processing of your information; or correct inaccurate or outdated personal information in our systems. We are seeking a highly skilled licensed psychologist with exceptional clinical expertise, writing skills, and content development experience who is passionate about developing client-facing materials (articles, quick tips, short psychoeducational videos, etc.) that teach evidence-based mental health skills.
NewHealth Industry - Clinical Management Senior Manager Accenture PlcHealth Industry - Clinical Management Senior ManagerSan Francisco, CALead with the Best: Join an industry-recognized healthcare consulting leader with a global team of over 20,000 professionals, collaborating to drive large-scale healthcare transformation across the globe. Continuous Learning & Growth: Take advantage of unmatched professional development opportunities, including interactive courses, real-world client simulations, and ongoing mentoring, to expand your healthcare consulting expertise.
Senior Clinical Trial Manager, Oncology Eikon Therapeutics, Inc.Senior Clinical Trial Manager, OncologyMillbrae, CA$143,000–$173,250 / yearThis role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our Jersey City, NJ or Millbrae, CA offices to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration. The successful candidate will need minimal oversight, will work closely with cross-functional teams to ensure successful completion of studies within timelines and budget, with a focus on exquisite quality to support excellence and world class clinical study management.
Senior Manager/Associate Director Clinical Monitoring Strategy & Optimization Oruka Therapeutics IncSenior Manager/Associate Director Clinical Monitoring Strategy & OptimizationMenlo Park, CARemote$161,000–$187,000 / yearSupport development and review of key study documents including Monitoring Plans, Risk Management Plans, Study Oversight Plans, Clinical Trial Management Plans, and Site Management Plans. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year.
Clinical Social Worker UCSF Medical CenterClinical Social WorkerSan Francisco, CACSWII: Master's degree in social work, psychology or related field from an accredited university and possession of the requirements necessary for application for licensure (as LCSW, LMFT or LPCC) as determined by the California Board of Behavioral Science; and knowledge and abilities essential to the successful performance of the duties assigned to the position. LICENSES AND/OR CERTIFICATIONS: CSW I: Master's degree in social work, psychology or related field from an accredited university, registered or eligible to register with the California Board of Behavioral Sciences (as ASW, AMFT, or APCC), and knowledge and abilities essential to the successful performance of the duties assigned to the position.
Senior Clinical Data Scientist Unlearn.AI IncSenior Clinical Data ScientistSan Francisco, CACollaborate closely with cross-functional teams of data scientists, machine learning scientists, engineers, and clinicians to design, build, and maintain robust data products grounded in sound data organization, domain knowledge, and careful analysis. Working in close collaboration with machine learning scientists, engineers, clinical scientists, and product partners, they transform complex clinical data into high-quality, well-understood datasets tailored for modeling and other downstream applications.