Lab Supervisor – Molecular Genetic Pathology and Clinical Genomics Stanford Health CareLab Supervisor – Molecular Genetic Pathology and Clinical GenomicsPalo Alto, CaliforniaSupervises the work of laboratory personnel engaged in performing routine and specialized technical procedures, including planning day to day laboratory work activities, evaluating work performed and handling procedural technical and non-technical laboratory problems. Under the guidance of the section Medical director, develops and implements department specific processes/procedures and quality control programs to ensure reliability of testing procedures, proper function of laboratory equipment, and compliance to safety/health and state/federal/licensing regulations.
Clinical Lab Scientist (CLS) Stanford Health CareClinical Lab Scientist (CLS)PALO ALTO, CA$69.10–$77.81 / hourUnderstands and applies the correct control measures and protocols in cases of abnormal results, reporting any discrepancies to a Senior, Reference, or Supervising Clinical Laboratory Scientist. Performs maintenance and function checks on analytical equipment and perform operational checks necessary for proper test performance to assure accurate and reliable test results and reporting.
Clinical Trial Manager Braveheart BioClinical Trial ManagerSan Francisco, California$140,000–$170,000 / yearPerform accompanied visits (PSSVs, SIVs, RMVs) with CRO CRAs to ensure study procedure conduct is in accordance with SOPs and protocol procedures and review routine regulatory documents/files in compliance with protocol, regulatory requirements, SOPs, and Monitoring Plan, as required. Our lead product candidate, BHB-1893, is a next-generation oral small-molecule cardiac myosin inhibitor (CMI) being developed for the treatment of obstructive HCM (oHCM) and non-obstructive HCM (nHCM).
Clinical Genetic Molecular Biological Scientist Trainee CareDx IncClinical Genetic Molecular Biological Scientist TraineeBrisbane, CAA CGMBS Intern performs laboratory duties under the supervision of a licensed CLS or the Clinical Laboratory Manager (CLM) and/or designee, who provides specific instruction and training regarding molecular techniques and bench tasks that are to be completed. The Clinical Genetic Molecular Biological Scientist Trainee (CGMBS Intern) performs a variety of laboratory and administrative tasks to obtain practical training hours in the CLIA-certified clinical laboratory here at CareDx.
NewMedical Director, Clinical Development(Nephrology) Jade BiosciencesMedical Director, Clinical Development(Nephrology)San Francisco, CaliforniaRemote$270,000–$300,000 / yearEducate and advise clinical sites/investigators to support enrollment and optimal study conduct, including presenting at investigator meetings and/or site initiation visits, and serving as the medical point of contact for site staff questions about patient eligibility, and providing input into patient safety assessment and management. Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases.
Clinical Trial ManagerNewHybrid Berkeley California United States Remote Caribou Biosciences IncClinical Trial ManagerNewHybrid Berkeley California United States RemoteBerkeley, CARemote$160,000–$175,000 / yearCollaborate effectively with Clinical Development, Data Management, Biostatistics, Regulatory Affairs, Medical Monitoring, Drug Supply, Quality Assurance, Safety, and other cross-functional partners to ensure successful trial execution. We believe the future of cell therapy is off-the-shelf, and we are advancing our pipeline of off-the-shelf, or allogeneic, cell therapies from our CAR-T cell therapy platform as readily available treatments for patients with hematologic malignancies and autoimmune diseases.
Medical Writer / Clinical Document - Remote YO AI LabsMedical Writer / Clinical Document - RemoteSan Jose, CARemote$50–$80 / hourWe are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.
Clinical Document Author - Remote YO AI LabsClinical Document Author - RemoteSan Francisco, CARemote$50–$80 / hourWe are seeking an experienced Medical Writer / Clinical Document Author to develop, review, and evaluate clinical and regulatory documents while ensuring scientific accuracy, regulatory compliance, and high-quality medical writing. Verify scientific accuracy using source data, TFLs (Tables, Figures, and Listings), and study documentation.
Clinical Lab Aide II CareDx IncClinical Lab Aide IIBrisbane, CA$23–$29 / hourThrough our innovative portfolio of molecular diagnostics, digital health solutions, AI-powered data and analytics, and patient support services, we partner with healthcare providers, patients, and biopharma organizations to help inform clinical decision-making and improve patient outcomes. A CLA performs laboratory duties under direct and constant supervision of a licensed CLS or the Clinical Laboratory Manager (CLM) and/or designee, who provides specific instruction regarding how tasks are to be completed and defines the steps to be employed.
Senior Manager, Data Engineering Stanford Health CareSenior Manager, Data EngineeringPalo Alto, CA$83.98–$111.27 / hourStakeholder Collaboration and Project Management: Partner with key stakeholders across Stanford Medicine (Stanford Health Care, Stanford School of Medicine, and Stanford Medicine Partners), including data scientists, analysts, clinical leaders, and researchers, to translate data needs into technical requirements. Essential Functions: Team Leadership and Development: Lead, mentor, and manage multiple teams of data engineers, providing technical guidance, career development, and performance management.
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) Medpace, Inc.Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)San Francisco, CaliforniaRemoteOn-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Laboratory Associate I, Pre-Clinical Synthego CorpLaboratory Associate I, Pre-ClinicalRedwood City, CA$27–$28 / hourDriven by a visionary approach, we strive to accelerate the therapeutic development process with best-in-class CRISPR solutions, simplified licensing & expert guidance, driving the adoption and success of CRISPR-based therapies to benefit all patients. Synthego is a pioneering force in the biotechnology industry, dedicated to advancing the frontiers of CRISPR cell and gene therapies through cutting-edge CRISPR technology and expertise.
Senior Research Associate KariusSenior Research AssociateRedwood City, CA$88,200–$102,900 / yearBy unlocking the information present in microbial cell-free DNA, we're helping doctors quickly solve their most challenging cases, providing industry partners with access to the microbial landscape to accelerate biomarker discovery and clinical trials, discover novel microbes, to ultimately reduce patient suffering worldwide. The company's platform is already delivering unprecedented insights into the microbial landscape, providing clinicians with a comprehensive test capable of identifying more than a thousand pathogens directly from blood, and helping industry accelerate the development of therapeutic solutions.
Senior Director, Pharmacovigilance Braveheart BioSenior Director, PharmacovigilanceSan Francisco, California$230,000–$325,000 / yearThe role will also serve as the operational pharmacovigilance lead for Braveheart's global co-development partnership, ensuring effective safety governance, implementation and oversight of Safety Data Exchange Agreements (SDEAs) and Pharmacovigilance Agreements (PVAs), management of safety data exchange and reconciliation activities, and alignment of safety surveillance, aggregate reporting, and benefit-risk assessments across global development programs. The Senior Director, Pharmacovigilance (PV) will serve as a key leader within Braveheart Bio's Drug Safety and Pharmacovigilance organization, partnering closely with the Vice President, Drug Safety and Pharmacovigilance to execute the company's global drug safety and pharmacovigilance strategy and ensure excellence in pharmacovigilance operations, safety surveillance, signal management, aggregate reporting, vendor oversight, and regulatory compliance.
NewSenior Specialist I, Patient Safety & Pharmacovigilance Clinical Trial Safety Operations Corcept Therapeutics IncSenior Specialist I, Patient Safety & Pharmacovigilance Clinical Trial Safety OperationsRedwood City, CA$103,600–$137,100 / yearWith advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today. This role supports Patient Safety and Pharmacovigilance (PSPV) Safety Operations by ensuring the quality, compliance, and timely reporting of safety information from company-sponsored clinical trials, Investigator-Initiated Studies, and expanded access/compassionate use programs.
Quality Assurance Manager (Clinical) InClinQuality Assurance Manager (Clinical)San Mateo, CARemote$100,000–$136,000 / yearAudit & Inspection Leadership: Perform audits and maintain Annual Audit Plans for internal departments, CROs, specialty service providers (EDC, e-diaries, IVRS), and clinical studies. You will lead audits, manage our eQMS, oversee CAPA management, and champion a culture of continuous improvement across the organization—all from the comfort of your home office.
Manager, Clinical Lab Management Nektar TherapeuticsManager, Clinical Lab ManagementCA$150,000–$185,000 / yearNektar currently anticipates the base salary for the Manager, Clinical Data Management to range from $150,000 to $185,000 for candidates in the Bay Area and will depend, in part, on successful candidate''s location and qualifications for the role, including education and experience. This role ensures the timely delivery of high-quality biological samples used to evaluate drug efficacy and is an integral member of the study team across study start-up, conduct, and close-out.
NewOphthalmic Sonographer - Eye Clinic Watson - Full Time(SEIU) Stanford Health CareOphthalmic Sonographer - Eye Clinic Watson - Full Time(SEIU)Palo Alto, California$48.25–$54.15 / hourCLINICAL DUTIES:• Perform ophthalmic photographic procedures such as optical coherence tomography, fundus photography, disc photography, fluorescein angiography, indocyanine green angiography, endothelial microscopy, slit lamp photography, gonio photography, and external photography to assist in the diagnosis of ocular pathology.• Practice at the leading edge of ophthalmologyWork alongside renowned specialists in an integrated network of vision care experts, supported by advanced technology and innovative facilities, including our Advanced Diagnostic Imaging Center and Eye Laser Center.
Clinical Research Coordinator II - The Nallamshetty Lab PAVIRClinical Research Coordinator II - The Nallamshetty LabPalo Alto, CAFull timeDesiredDegree in related field;Experience with grants and contracts function, clinical trial and research data management;Experience coordinating clinical research studies, recruiting research participants, collecting research data, and working with regulatory requirements;Knowledge of clinical research principles, Good Clinical Practice (GCP), human subjects protections, and research ethics gained through education or experience. The position works closely with the Principal Investigator, study team, sponsors, regulatory bodies, and research participants to ensure studies are conducted in accordance with study protocols, Good Clinical Practice (GCP), institutional policies, and federal regulations.
Product Counsel Doximity IncProduct CounselSan Francisco, CA$184,000–$214,000 / yearYou will sit with the engineers, data scientists, and product managers building our clinical AI products - ambient documentation, clinical search and answers, and AI-powered clinician workflows - and help them ship quickly and responsibly. As a Product Counsel, R&D / AI, you will: Act as embedded counsel to our AI and R&D teams, advising on product design, model development, and launch decisions from concept through release - and owning the most significant legal questions our AI organization faces.