Clinical Trial Assistant (CRA) - U.S. Based IceCure Medical LtdClinical Trial Assistant (CRA) - U.S. BasedCAYou will be responsible for coordinating clinical study activities, supporting and monitoring research sites, maintaining high-quality clinical documentation and data, and ensuring compliance with protocols, GCP and applicable regulations. Work collaboratively with the Clinical Operations team, CRO, Data Management, Regulatory, Quality, Safety, and other cross-functional stakeholders to ensure effective study execution, timely resolution of issues, and achievement of study milestones.
Program Coordinator II, Community Based Research Initiative (Community Engagement & Research Coordination) Charles R. Drew UniversityProgram Coordinator II, Community Based Research Initiative (Community Engagement & Research Coordination)Los Angeles, CaliforniaOversee the online engagement platform, participant communications, scheduled calls, and data-capture elements for the digitally delivered programs (INSPIRE CA, and USA), coordinating closely with the technology team to ensure the platforms function reliably and participant data is captured accurately and securely. INSPIRE Faith is a deep, place-based partnership with faith institutions requiring regular in-person engagement with community partners; INSPIRE CA, and INSPIRE USA are digitally delivered, largely automated programs conducted primarily online, with select live sessions led by physicians and study staff.
Clinical Informaticist - Epic Cupid - IT-Clinical Rady Children's HospitalClinical Informaticist - Epic Cupid - IT-ClinicalCA$48.03–$66.06 / hourUnderstanding of health care patient administration, clinical and business systems and must have installed a minimum of one computer-based hospital system and actively performed the following: process and workflow analysis, systems/applications analysis, project lifecycle implementation with in-depth experience and training in a minimum of four discreet major projects. Must possess skills and experience in oral and written communications; This is applicable to analysis documentation, project management deliverables and documentation, application/systems specifications, project preparation, risk identification and escalation; Ability to present to a broad spectrum of individuals and groups including senior management, physicians and health care professionals.
Licensed Clinical Social Worker II-Clinical Supervisor Braille Institute Of America, Inc.Licensed Clinical Social Worker II-Clinical SupervisorLos Angeles, CA$95,000–$110,000 / yearThrough our 2025-2027 strategic planning process, we identified the next generation opportunities to advance critical initiatives in areas such as customer research; the expansion and transformation of current programs and services; the development of new nationally and internationally accessible programs; the creation of dynamic new strategic partnerships; and the alignment of our mission, strategy, and resources. Job Summary: Braille Institute of America is seeking an experienced Licensed Clinical Social Worker to oversee clinical service delivery within the social work program throughout our Southern California Centers and national online programming.
Bilingual Research Associate (English and Mandarin) Parexel International CorpBilingual Research Associate (English and Mandarin)Glendale, CA$20–$25 / hourRecruit study participants by calling the database, attending company sponsored community events, posting flyers in schools, senior centers, supermarkets, and other establishments. Conduct screening visits and study protocol specific study participant visits, assist staff physicians in assessment of concomitant medications, adverse events, lab results, and other test results.
Research Assistant MemorialCare Health SystemResearch AssistantFountain Valley, CA$24.01–$34.81 / hourUnder direct supervision of the Director of Clinical Operations, Manager(s) of Clinical Operations and Principal Investigator, the Research Assistant is responsible for helping enlist, maintain, and assure protocol compliance for all study participants in assigned clinical research protocol(s). MemorialCare is a nonprofit integrated health system that includes four leading hospitals, award-winning medical groups consisting of over 200 sites of care, and more than 2,000 physicians throughout Orange and Los Angeles Counties.
NewOncology Research Scribe Flourish ResearchOncology Research ScribeCentury City, CA$22–$26 / yearBy ensuring visit notes, orders, and follow-up items are captured completely and correctly the first time, the Scribe directly supports faster patient throughput, stronger protocol compliance, and a smoother experience for patients considering or enrolled in a clinical trial. The Oncology Research Scribe works alongside research oncologists and study staff during patient visits to capture accurate, timely clinical documentation in the EMR and study source.
Staff Research Associate 3 UCLA Health SystemStaff Research Associate 3Los Angeles, CA$75,439.44–$121,333.68 / yearWorking closely with faculty, researchers, trainees, and external collaborators, the SRA III will contribute to the development of innovative assays, generation of high-quality research data, and advancement of scientific publications and grant-funded projects. The successful candidate will manage and maintain state-of-the-art instrumentation, perform quality control and data analysis, and oversee essential laboratory operations such as inventory management, reagent procurement, regulatory compliance, and equipment maintenance.
Research Assistant Flourish ResearchResearch AssistantCentury City, CA$21–$32 / yearVCT was founded by leading Clinical Oncologist, Dr. David Berz, and has multiple sites spanning California in Century City, Panaroma City, and Murrieta, and has recently expanded to Denver, Colorado. Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research.
Laboratory Research Associate Charles R. Drew UniversityLaboratory Research AssociateLos Angeles, CaliforniaThis role is essential to maintaining the integrity and consistency of the laboratory's scientific output across both the in vivo and in vitro arms of the research program, which spans exosome biology, cancer metabolism, and small-molecule drug discovery in breast cancer and acute myeloid leukemia. Under the direct supervision of the Principal Investigator, Dr. Qiongyu Hao, the Laboratory Research Associate supports both the animal colony operations and the routine bench work of the laboratory's translational cancer research program.
Staff Research Associate 3 University of CaliforniaStaff Research Associate 3Los Angeles, CA$75,439.44–$121,333.68 / yearWorking closely with faculty, researchers, trainees, and external collaborators, the SRA III will contribute to the development of innovative assays, generation of high-quality research data, and advancement of scientific publications and grant-funded projects. The successful candidate will manage and maintain state-of-the-art instrumentation, perform quality control and data analysis, and oversee essential laboratory operations such as inventory management, reagent procurement, regulatory compliance, and equipment maintenance.
CON-Research Associate 1 Xencor IncCON-Research Associate 1Pasadena, CA$33.50–$40 / hourJob Duties Include: Perform molecular biology workflows, including molecular cloning (subcloning, site-directed mutagenesis, and Gibson Assembly), primer design, bacterial transformation, plasmid DNA preparation, linear expression cassette generation, and PCR/qPCR optimization and troubleshooting. Familiarity with AI tools and the ability to use them in a compliant and responsible manner, including validating outputs, mitigating risks, actively reinforcing responsible use across teams, and ensuring strict adherence to company policies and regulatory requirements.
NewResearch Scientist, Biomarker Sciences I* MindlanceResearch Scientist, Biomarker Sciences I*Santa Monica, CA$46–$47.35 / hourRegulatory filing experience and a demonstrated ability to facilitate clinical trial execution, synthesize scientific data, communicate key findings cross-functionally is required. Collaborates with Clinical development teams including Clinical Operations, Regulatory, Clinical Data Management and Biometrics/Stats to advance data acquisition and analyses of clinical trial data.
NewNurse Practitioner- Research -Per Diem University of CaliforniaNurse Practitioner- Research -Per DiemLos Angeles, CAIn the Research NP role, the NP will promote the ethical care of research patients and liaison with principle investigators to care for clinical trial patients, as well as provide education and support, make appropriate referrals and document services rendered. By using the SPs the NP is able to change treatment regimen after observing signs and symptoms of illness, reactions to treatment, general behavior and physical condition, and determines if they are abnormal findings (Ca Nursing Practice Act, subsection(b) of Section 2725).
NewResearch Scientist-Multiple Myeloma Net2SourceResearch Scientist-Multiple MyelomaSanta Monica, CA$43.17–$47.36 / hourRegulatory filing experience and a demonstrated ability to facilitate clinical trial execution, synthesize scientific data, communicate key findings cross-functionally is required. Education Level Advanced scientific degree (i.e. MD, PharmD, PhD) and 3+ years in industry OR Master's Degree and 5+ years of scientific experience OR Bachelor's Degree and 7+ years of scientific experience.
RN Clinical - 5 E Tele - Full Time 12 Hour Days (Non-Exempt) (Union) University of Southern CaliforniaRN Clinical - 5 E Tele - Full Time 12 Hour Days (Non-Exempt) (Union)Los Angeles, CA$45.76–$98.80 / hourOBSERVES REGULATORY AGENCY REQUIREMENTS: National Patient Safety Goals Patient identifiers Unapproved abbreviations Universal Protocol (Procedural Time Out) Hand-Off Medication Reconciliation Clinical Alarms Other Hazardous waste management Biohazard Medication Sharps HIPAA OSHA requirements (i.e. no food or drink in clinical areas) JCAHO - continuous survey readiness Critical Values Write Down Read Back Follow up Telephone order Appropriate Documented Signed, Timed and Dated Stamped Entered into unit log Maintains safe practice in the work environment Correct body mechanics Electrical safety Infection Control Procedures Hand Washing. DOCUMENTATION Documentation is complete and correct on all flow sheets and chart forms: Admission Assessment Pain scale assessment and reassessment before and after intervention Daily flow sheet Restraint flow sheet Diabetes flow sheet Educational flow sheet Kardex Care Plan Risk Assessment & Reassessment upon Fall MAR Equipment & Supplies Intra and Inter Facility Transfer Forms Belonging Tracking Form Ensures orders are transcribed and signed off prior to the end of the shift.
RN Clinical - 5 E Tele - Part Time 12 Hour Days (Non-Exempt) (Union) University of Southern CaliforniaRN Clinical - 5 E Tele - Part Time 12 Hour Days (Non-Exempt) (Union)Los Angeles, CA$45.76–$98.80 / hourOBSERVES REGULATORY AGENCY REQUIREMENTS: National Patient Safety Goals Patient identifiers Unapproved abbreviations Universal Protocol (Procedural Time Out) Hand-Off Medication Reconciliation Clinical Alarms Other Hazardous waste management Biohazard Medication Sharps HIPAA OSHA requirements (i.e. no food or drink in clinical areas) JCAHO - continuous survey readiness Critical Values Write Down Read Back Follow up Telephone order Appropriate Documented Signed, Timed and Dated Stamped Entered into unit log Maintains safe practice in the work environment Correct body mechanics Electrical safety Infection Control Procedures Hand Washing. DOCUMENTATION Documentation is complete and correct on all flow sheets and chart forms: Admission Assessment Pain scale assessment and reassessment before and after intervention Daily flow sheet Restraint flow sheet Diabetes flow sheet Educational flow sheet Kardex Care Plan Risk Assessment & Reassessment upon Fall MAR Equipment & Supplies Intra and Inter Facility Transfer Forms Belonging Tracking Form Ensures orders are transcribed and signed off prior to the end of the shift.
NewResearch Scientist, Multiple Myeloma - Translational Medicine ICONMA, LLCResearch Scientist, Multiple Myeloma - Translational MedicineSanta Monica, CA$42.35–$47.35 / hourRegulatory filing experience and a demonstrated ability to facilitate clinical trial execution, synthesize scientific data, communicate key findings cross-functionally is required. Collaborates with Clinical development teams including Clinical Operations, Regulatory, Clinical Data Management and Biometrics/Stats to advance data acquisition and analyses of clinical trial data.
Senior Patient Recruitment Specialist Flourish ResearchSenior Patient Recruitment SpecialistCovina, CA$31–$33 / hourRepresent Flourish Research in a professional and courteous manner (verbal, written and in appearance) when interacting with Flourish staff, sponsors, contract research organizations (CROs), IRBs, participants, nursing and medical staff members of various clinics, hospitals, and physician’s offices; Flourish Research contract personnel, as well as any other person(s) when carrying out task and responsibilities. To obtain clean, objective, and accurate data while following applicable Flourish SOPs, policies and procedures, federal regulations, medical ethics, Good Clinical Practices (GCPs), International Council of Harmonization (ICH), Institutional Review Board (IRB) requirements, and in compliance with specific sponsor protocol requirements.
Feasibility Informatics Manager ICON PlcFeasibility Informatics ManagerLong Beach, CARelevant parties include, but are not limited to: Proposal team members, Project Managers/Strategy Leads, Patient Recruitment & Retention Specialists, Site Identification Managers/Leads, Therapeutic Experts, Therapeutically Aligned clinical teams (as assigned), Business Development Associates, Sponsors, Quality Assurance Associates, and other internal/external experts. Role Summary: To serve as a technical feasibility strategy expert, leading and managing the process of clinical project feasibility in support of proposal teams by assisting Business Development with the generation of cost proposals, providing input and advice relating to operational strategy, and supporting client interactions and long-term strategic partnerships.