Operator 1, Packaging Operations Katalyst Healthcares & Life SciencesOperator 1, Packaging OperationsSan Diego, CALearn and understand: Basic Packaging process flow, Basic Inventory and supplies management process flow, Basic bottling techniques for all single vial purified and conjugate materials, Basic packaging processes including bagging and labeling, Use of pipette, scale and other packaging equipment as required, Support label creation process by learning and operating all labeling equipment. The packaging technician gathers the materials required for their order: liquid bulk reagent (antibody or buffer), vials/bottles, caps, paperwork, labels and prepares and organizes the starting materials accurately and then presents the production order setup for line clearance.
Manager, Clinical Quality System Documents Arrowhead PharmaceuticalsManager, Clinical Quality System DocumentsSan Diego, CA$120,000–$145,000 / yearLead and coordinate document activities with cross-functional business stakeholders, including Clinical Operations, Drug Safety/Pharmacovigilance, Biometrics, Clinical Data Management, Clinical Development/Medical, Regulatory Affairs, Medical Writing, Clinical Supply Management and Clinical Quality Assurance, ensuring timely completion of document deliverables. Support QMS Quality Assurance (QA) counterparts in executing document control workflows by coordinating and facilitating the development, review, revision, approval, issuance, periodic review, and retirement of controlled documents across Clinical Development functions, ensuring timely completion and compliance with established document control processes.
Staff Program Manager, Clinical Sequencing CDx Thermo Fisher ScientificStaff Program Manager, Clinical Sequencing CDxCarlsbad, CaliforniaDemonstrated experience managing strategic biopharma, biotechnology, customer, clinical, CRO, or technology-partner relationships, including expectation-setting, commitment negotiation, escalation management, and resolution of competing priorities across internal teams, clinical sites, laboratories, consultants, and vendors. Working knowledge of regulated product development sufficient to plan and govern execution, including 21 CFR Part 820 design controls, ISO 13485 principles, clinical/analytical validation, risk management, traceability, and quality systems.
Clinical Data Scientist Exagen Diagnostics IncClinical Data ScientistCarlsbad, CA$130,000–$160,000 / yearProvide clinical data management for studies sponsored by the Company and studies where Exagen serves as a central laboratory, including data management plans, data reconciliations, release of data clarification forms, query resolution, dataset locks, manual release of test reports, and preparation of reports for invoicing, in coordination with study sponsors and/or CROs. The CDS owns dataset curation and clinical database development across the Company's registry, biobank, and study data; applies machine learning and AI approaches-including large language model (LLM)-assisted workflows-in partnership with the data science team; and delivers analysis-ready data to biostatistics.
Temporary Toxicology Operations Associate Ionis Pharmaceuticals Inc.Temporary Toxicology Operations AssociateCarlsbad, CA$39.73–$52.48 / hourWith multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals. General operational support including document processing (e.g., ELN, study tracker management, etc.), maintaining file systems for accuracy and completeness, invoice review and approval, REQUIREMENTS: A bachelor's degree in biology or a related science field is required along with a minimum of 5 years relevant experience.
Sr. Clinical Research Associate (In-house) Artiva Biotherapeutics IncSr. Clinical Research Associate (In-house)San Diego, CA$110,000–$135,000 / yearMay review and approve trip reports, track data query reports, site visit metrics, and overall site performance May perform routine monitoring at limited clinical sites May perform site initiation, routine monitoring and close-out visits at a limited # of clinical sites, as well as co-monitoring with local CRAs Ensures quality of the data generated from clinical sites and assists in resolving subject eligibility and protocol deviation issues May assist in the preparation of, and may present at investigator vendor meetings and workshops Actively involved in the performance of study feasibility assessments Provides rapid action to address both internal and site QA findings from audits Coordinate the activities from third party vendors including metrics, accruals, process planning, and implementation Routinely participates in department and clinical trial team meetings and participates in collaborative efforts (e.g. This includes two company-sponsored trials, one in systemic lupus erythematosus for patients with or without lupus nephritis, and a basket trial across autoimmune diseases (Rheumatoid Arthritis, Systemic Sclerosis, Idiopathic Inflammatory Myopathies and Sjögren's Disease), as well as an investigator-initiated basket trial in B-cell driven autoimmune diseases.
Project Manager - Clinical Projects - San Diego PolyPeptide USProject Manager - Clinical Projects - San DiegoSan Diego, CaliforniaYou will help turn customer agreements into clear action plans, guide cross-functional teams through complex deliverables, and play a direct role in supporting programs tied to important pharmaceutical and biotech development. In this role, you will be at the center of clinical project execution, partnering with customers, internal technical teams, Supply Chain, Commercial Operations, Quality, and Site Leadership to keep projects moving forward.
Associate Director, Clinical Trial Management Xencor IncAssociate Director, Clinical Trial ManagementSan Diego, CA$169,500–$203,250 / yearLeads a cross-functional study team to ensure all elements of the study are addressed proactively by the relevant parties, follows up on action items, proactively identifies and resolves operational issues and is accountable for the overall study performance, budget and timeline in accordance with the company corporate goals. Education/Experience/Skills: Position requires a Bachelor's degree in a field of science (such as Biology or Immunology) and at least 10 years of related experience, including 6 years in clinical trial management/clinical operations departments.
Director, Clinical Science Janux Therapeutics Inc.Director, Clinical ScienceSan Diego, CA$236,000–$255,000 / yearAn integral member of the Janux Therapeutics' Clinical Development team; the Director, Clinical Science will support the strategic planning and execution of clinical-stage programs for one of the the company's early stage oncology platforms. Perform clinical data review and identify clinical data insights through ongoing patient level review and trends analysis, working cross-functionally to monitor clinical data.
Clinical Lab Scientist - Microbiology LabCorpClinical Lab Scientist - MicrobiologySan Diego, CA$50–$58 / hourAs we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes.
Senior Clinical Research Coordinator Headlands Research IncSenior Clinical Research CoordinatorEscondido, CA$80,000–$90,000 / yearIf you're an experienced Clinical Research Coordinator who values strong operations, multidisciplinary collaboration, and a schedule that actually supports work-life balance, AMCR Institute may be the right next step in your career. Headlands Research AMCR Institute, located in Escondido, California, is dedicated to advancing metabolic and immunologic research through patient-centered, high-quality clinical trials.
Clinical Quality Assurance, Specialist II Arrowhead PharmaceuticalsClinical Quality Assurance, Specialist IISan Diego, CA$80,000–$95,000 / yearKey responsibilities include assisting in GCP Quality Event management (non-conformances, deviations, CAPAs), contributing to risk-based audit planning, support in audits and inspections, SOP review and collaborating closely with the Clinical Operations team to ensure GCP compliance and data integrity. This includes support in investigator audit programs, risk management plans, regulatory inspections, generating metrics for continuous improvement, and quality events while collaborating cross-functionally to uphold clinical trial quality and regulatory compliance.
Contractor- Clinical Research Coordinator (San Diego, CA) Profound Research LLCContractor- Clinical Research Coordinator (San Diego, CA)San Diego, CAYou'll help manage study activities, lead participant visits, complete protocol-required procedures and documentation, and work closely with investigators, sponsors, CROs, and internal teams. This is a 1099 independent contractor opportunity designed to support current high-volume vaccine study needs while giving the right person a chance to learn, contribute quickly, demonstrate ownership, and be considered for future opportunities.
CCC Clinical Trainer VITAS Healthcare CorpCCC Clinical TrainerSan Diego, CAMonitor new agent calls and data processing during the new hire period, pre and post formal training and education, to ensure on-going call handling improvement, the integrity of the data collection, and superior customer service is being delivered. The VITAS Healthcare CCC Clinical Trainer is responsible for facilitating and supporting the training, education and on-going development of PCC's, LPN's, RN's within their initial 90 days of employment and beyond.
Rebate Clinical Program Manager (PharmD) MedImpactRebate Clinical Program Manager (PharmD)San Diego, CaliforniaOther activities are centered on client specific requests and involve production of reports and providing financial and drug utilization data that assist the state(s) in determining their financial solvency, drug purchasing policies and allocation of received rebate monies. One must be able to; manage difficult or emotional client situations; Respond promptly to client needs; Solicit client feedback to improve service; Respond to requests for service and assistance from clients; Meet commitments to clients.
Clinical Lab Scientist - Microbiology Labcorp Holdings IncClinical Lab Scientist - MicrobiologySan Diego, CA$50–$58 / hourAs we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes.
Clinical Laboratory Scientist - Profile Chemistry Labcorp Holdings IncClinical Laboratory Scientist - Profile ChemistrySan Diego, CA$50–$58 / hourAs we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes.
Clinical Research Coordinator II Headlands Research IncClinical Research Coordinator IISan Diego, CA$70,304–$75,000 / yearManaging all aspects of a study including participating in the informed consent process, coordinating and performing all visit study procedures per the protocol, entering data and query resolution, Investigational Product management, and managing all study related supplies and equipment, hosting monitoring visits, and attending Investigator Meetings. Under the supervision of the Site Director, the Senior Clinical Research Coordinator is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines.
Associate Director, Clinical Development - Neurology Ionis Pharmaceuticals IncAssociate Director, Clinical Development - NeurologyCarlsbad, CA$168,820–$250,502 / yearRESPONSIBILITIES: Serve as the clinical lead for assigned studies, representing Clinical Development in internal and external interactions and helping ensure successful execution of a high-priority Phase 3 program by: Developing and maintaining excellent working relationships with investigators and clinical trial teams. With multiple marketed medicines and a leading pipeline in neurology, cardiology and select areas of high patient needs, we continue to drive innovation in RNA therapies in addition to advancing new approaches in gene editing to provide greater value to patients and are well positioned financially to deliver on our strategic goals.
NewClinical Supervisor GeneralClinical SupervisorEscondido, CaliforniaOur unique campus features residential staff and house parents serving as surrogate parents who mentor and tutor students, teach age-appropriate independent living skills, create opportunities to explore new interests, encourage participation in sports and recreation, assist in the exploration of career and job opportunities, and promote family living skills. They must meet the Board of Behavioral Sciences requirements to provide clinical supervision, which includes completing the initial 15 hours of supervision training and coursework, as well as six hours of supervision training during each renewal period while supervising trainees or associates.