NewPart-Time Clinical Dietitian AramarkPart-Time Clinical DietitianLos Angeles, CABENEFITS : Aramark offers comprehensive benefit programs and services for eligible employees including medical, dental, vision, and work/life resources. Provide education and counseling to patients and their families on proper nutrition, healthy eating habits, and lifestyle changes.
Clinical - Assoc Spec, Clinical Research MindlanceClinical - Assoc Spec, Clinical Researchirvine, CA$43.56–$45.37 / hourConduct in-house and site (if applicable) reviews of associated documentation and participate in internal and competent authority (e.g., FDA, DEKRA, PMDA) audits to ensure all essential clinical Trial Master File (TMF) documents are compliant with Good Documentation Practices, Edwards internal SOPs, and US and OUS regulations. Summary: The main function of a clinical research specialist is to perform study start-up and conduct activities including ICF review that meets regulatory requirements, creating study specific essential document lists, managing and communicating the status of study progress and activities.
Clinical Research Program Manager Charles R. Drew UniversityClinical Research Program ManagerLos Angeles, California$75,700–$90,000 / yearThe Clinical Research Program Manager works closely with the Director, Principal Investigators (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to manage the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support. Ability to develop and maintain professional working relationships in complex program/organizational settings involving heterogeneous constituents such as academic and clinical faculty, staff, students, and community partners from diverse backgrounds.
NewTMS Clinical & Research Service Manager University of CaliforniaTMS Clinical & Research Service ManagerLos Angeles, CA$42.58–$91.14 / hourUCLA Health's Neuromodulation Division is seeking to hire a TMS Clinical & Research Services Manager to provide operational leadership for Transcranial Magnetic Stimulation (TMS) services and clinical research programs. You will be responsible for overseeing complex clinical operations, research support functions, financial performance, regulatory compliance, and staff leadership across specialized treatment and research services.
Clinical Research Manager BiVACORClinical Research ManagerHuntington Beach, California$110,000–$150,000 / yearAs a Clinical Research Manager, you will own end-to-end US IDE study operations, leading a team of clinical research professionals, ensuring regulatory compliance across all active sites, and driving the clinical strategy that will help bring the world’s first Total Artificial Heart to patients who need it most. Collaborate on clinical strategy and author key clinical documents including clinical study protocols, clinical study reports, clinical evaluation plans/reports, annual progress reports, risk-benefit analyses, and clinical marketing materials.
Medical Assistant - Clinical Research (6:00 am - 6:00 pm) Clinical Innovation Inc.Medical Assistant - Clinical Research (6:00 am - 6:00 pm)Bellflower, CAPart timePreparing participant visits based on CRCs schedule, ensuring all source documents, assessments, lab kits and other visit materials are available and accurate. Provides direct support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing strict adherence to ICH, GCP, protocol, and site guidelines and policies.
Clinical Research Coordinator ATD Technology LLCClinical Research CoordinatorFullerton, CA$45Oncology Clinical Research Coordinator General Summary: Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. Minimum 2 years' experience in a clinical research setting where candidate managed patients (consent them, perform vitals/EKG, process labs, dispense medication, complete documentation, enter data).
Clinical Lab Scientist (CLS) - Automated Chemistry IQVIAClinical Lab Scientist (CLS) - Automated ChemistryValencia, CaliforniaJob Summary: Provide professional and technical expertise to perform automated and manual clinical laboratory testing within the Automated Chemistry area, ensuring accurate and timely results that support clinical research and patient care. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
NewResearch RN - Clinical Translational Research Center UCLA Health SystemResearch RN - Clinical Translational Research CenterLos Angeles, CA$65.76–$97.76 / hourDemonstrates responsibility for effect on others by respecting others' opinions and ideas, maintaining cooperative and collaborative relationships with co-workers, demonstrating professional control in stressful situations, and readily assisting co-workers while maintaining interdepartmental communication. Working under the guidance of the Unit Director, you will deliver exceptional direct patient care, collaborate with study teams to optimize protocol-specific workflows, and help advance promising innovations from bench to bedside.
Clinical Director Neurology UCLA Health SystemClinical Director NeurologyLos Angeles, CA$132,300–$307,100 / yearThis role is responsible for directing practice operations, supporting regional leadership, and partnering with physicians, practice managers, and staff to ensure exceptional patient care, operational excellence, quality outcomes, and an outstanding patient experience. In collaboration with executive and clinical leadership, you will foster a high-performing environment that supports innovation, clinical research, workforce development, and the delivery of world-class healthcare aligned with UCLA Health's mission and strategic objectives.
Clinical Operations Manager BiVACORClinical Operations ManagerHuntington Beach, California$118,000–$154,000 / yearAs Clinical Operations Manager, you will be the organizational backbone of site-level activity, ensuring every participating center is prepared, compliant, and ready to support patients receiving the world’s first Total Artificial Heart. This is a high-impact, cross-functional role at the heart of BiVACOR’s clinical program, where your operational expertise will directly shape the success of our first-in-human and pivotal clinical studies.
Sr. Clinical Research Coordinator - Hybrid University of California, IrvineSr. Clinical Research Coordinator - HybridOrange, CaliforniaFull timeThe incumbent is also responsible for maintaining communication with all elements of a multi-level research network, including attending Disease Oriented Teams (DOTs) meetings, interacting with sponsoring agencies including National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors. *Misconduct Disclosure Requirement: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer.
Clinical Trials Site Director - Multiple Locations Nationwide Headlands Research IncClinical Trials Site Director - Multiple Locations NationwideCAThis general interest posting is designed for Site Directors who may not see a current opening that aligns with their location-but who would like to be considered for future leadership opportunities across our growing network of clinical research sites nationwide. Our Site Directors play a critical role in driving site performance, leading cross-functional teams, and ensuring the successful execution of clinical trials in a compliant, patient-centered environment.
Lead Clinical Data Manager (Remote) IQVIA Holdings IncLead Clinical Data Manager (Remote)Anaheim, CARemote$86,800–$217,100 / yearYour previous roles/job titles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager. IQVIA is seeking experienced Senior Data Team Leads to oversee end-to-end data management delivery for global clinical trials.
Clinical Research Coordinator (Experienced) - Long Beach Irvine Clinical ResearchClinical Research Coordinator (Experienced) - Long BeachLong Beach, CA$30–$40 / hourFinal compensation offers will be determined based on the candidate's specific internal level (CRC II - IV), years of relevant clinical trial experience, and applicable clinical certifications (e.g., CCRC, nursing, or phlebotomy license). Technical Skills: Demonstrated ability to navigate complex clinical trial management systems (CRIO eSource & CTMS) and EDC platforms quickly and accurately.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedCA$71,900–$189,000 / yearEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Sr Clinical Research Associate - Oncology United BioSource LLCSr Clinical Research Associate - OncologyCARemoteBrief Description: Monitors clinical trials and observational studies ensuring protocol adherence, managing site activities, and overseeing data collection and integrity. Enters site visits, site monitoring reports, follow-up letter sent date and site contacts into UBC's Clinical Trial Management System (CTMS).
NewMobile Clinical Research Nurse - Chatsworth, CA Vita MobileMobile Clinical Research Nurse - Chatsworth, CAChatsworth, CAVitaMobile Medical Support Services has an urgent need for a per diem Registered Nurse to join our Clinical Research Team as a Mobile Clinical Research Nurse. Study visit activities include, but are not limited to: Scheduling visits with study participants.
Unit Director - Clinical and Translational Research Center (CTRC) University of CaliforniaUnit Director - Clinical and Translational Research Center (CTRC)Los Angeles, CA$148,700–$352,100 / yearThe UCLA Clinical and Translational Science Institute (CTSI) is seeking an experienced Nurse Director to lead operations for the UCLA Clinical and Translational Research Center (CTRC), a premier research unit supporting more than 400 active clinical trials. Possesses and applies the skills and knowledge necessary to provide care to patients throughout their participation in clinical trials, with consideration of aging processes, human development stages and cultural patterns in each step of the research study process, and consistent with unit guidelines and hospital policies, procedures and protocols.
Clinical Research Associate II Cedars-Sinai Medical CenterClinical Research Associate IILos Angeles, CADr. Tan, Associate Professor, Cancer Research Center for Health Equity, Division of Population Sciences, Department of Biomedical Sciences, is a social psychologist and applies her training in behavioral and prevention sciences to develop innovative interventions for improving health outcomes among marginalized populations in the U.S. This position provides contributions to behavioral and implementation science for the Cancer Research Center for Health Equity. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with all federal and local guidelines.