Clinical Research Nurse / Intermittent Parexel International CorpClinical Research Nurse / IntermittentGlendale, CA$40–$47 / hourPerform or arrange for phlebotomy, urine collection, sample preparation, storage and shipment of samples, drug dispensing, and follows GCP quality study documentation. In addition to base salary, some roles may be eligible for participation in Parexel's annual performance-based bonus plan, annual salary review and additional total rewards incentives.
Payer Stars/Quality Clinical Consultant, Senior Manager PwCPayer Stars/Quality Clinical Consultant, Senior ManagerLos Angeles, CA$124,000–$280,000 / yearAs a Payer STARS/Quality Clinical Consultant, Senior Manager, you will engage with clients in the health services sector, providing strategic guidance and operational consulting to enhance their clinical quality and performance metrics. PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy .
Payer STARS/Quality Clinical Consultant, Senior Manager PricewaterhouseCoopers LLPPayer STARS/Quality Clinical Consultant, Senior ManagerLos Angeles, CA$124,000–$280,000 / yearAs a Payer STARS/Quality Clinical Consultant, Senior Manager, you will engage with clients in the health services sector, providing strategic guidance and operational consulting to enhance their clinical quality and performance metrics. PwC does not intend to hire experienced or entry level job seekers who will need, now or in the future, PwC sponsorship through the H-1B lottery, except as set forth within the following policy: https://pwc.to/H-1B-Lottery-Policy .
Senior Oncology Clinical Research Associate Zp Group LlcSenior Oncology Clinical Research AssociateLos Angeles, CA$145,000–$175,000 / yearThe Senior Contract Oncology Clinical Research Associate (SCRA) will participate in ongoing Clinical Trials throughout the Country for a leading Clinical Research Organization. Responsibilities for the Senior Contract Oncology Clinical Research Associate: Conduct site and study visits and perform all site monitoring activities across multiple study.
NewClinical Research Coordinator Actalent IncClinical Research CoordinatorCerritos, CA$33–$40 / hourThis role focuses on screening, recruiting, and consenting patients, performing study-related patient visits and procedures, and collaborating closely with data and regulatory teams to ensure accurate documentation and compliance with study protocols. The Clinical Research Coordinator works within a collaborative oncology research team that includes full-time and part-time coordinators, research assistants, data management staff, regulatory staff, and project management support.
Clinical Research Coordinator ECN Operating LLCClinical Research CoordinatorNorthridge, CA$18–$19 / hourThe CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling. Candidates with current Phlebotomy certification or Medical Assistant (MA) certification are strongly preferred , as this role may include specimen collection and basic clinical procedures.
NewClinical Research Coordinator Avispa TechnologyClinical Research CoordinatorLos Angeles, CA$65 / hourCollaborate with investigators, sponsors, monitors, and research teams to support Phase I-IV, industry-sponsored, investigator-initiated, NIH-sponsored, interventional, observational, multicenter, and academic medical center research studies. Oversee daily operations of multiple clinical research studies, ensuring compliance with sponsor, institutional, FDA, GCP, and regulatory requirements throughout study start-up, maintenance, monitoring, and close-out activities.
NewClinical Research Coordinator Avispa Fukuoka Co LtdClinical Research CoordinatorLos Angeles, CACollaborate with investigators, sponsors, monitors, and research teams to support Phase I-IV, industry-sponsored, investigator-initiated, NIH-sponsored, interventional, observational, multicenter, and academic medical center research studies. Clinical Research Coordinator Responsibilities: Oversee daily operations of multiple clinical research studies, ensuring compliance with sponsor, institutional, FDA, GCP, and regulatory requirements throughout study start-up, maintenance, monitoring, and close-out activities.
Manager, Clinical Services, NICCU Children's Hospital Los AngelesManager, Clinical Services, NICCULos Angeles, California$151,861–$260,333 / yearFull timeThe role supports a 58-bed Level IV Neonatal and Infant Critical Care Unit (NICCU); one of the most advanced neonatal programs, providing care for the highest acuity neonatal and infant populations, including complex medical and surgical conditions. Overview: Purpose Statement/Position Summary: The Manager of Clinical Services assumes primary responsibility and oversight for all aspects of the work area, including establishing and maintaining the CHLA culture of care, as well as operational, clinical, and educational functions.
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.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedRedondo Beach, CA$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.
Clinical Research Coordinator I - Westside Los Angeles Irvine Clinical ResearchClinical Research Coordinator I - Westside Los AngelesLos Angeles, CAHours and Compensation This is a full-time employment position based in-person at our Inglewood Clinical / Westside Los Angeles site in Ladera Heights: 5120 W Goldleaf Cir, Ste 250, Los Angeles, CA 90056 The starting compensation for the role is $27/hr (approximately $56,160 per year). Our largest area of research is in Alzheimer’s Disease prevention and treatment drug trials, and our doctors were the largest contributors in the world to the most recently FDA-approved medication in Alzheimer’s Disease.
NewClinical Research Phlebotomist Assistant Actalent IncClinical Research Phlebotomist AssistantCerritos, CA$20–$25 / hourThe Clinical Research Assistant supports clinical research coordinators in the execution of oncology clinical trials by assisting with patient visits, collecting high-quality data, and contributing to regulatory and data management activities. The role is part of a collaborative clinical research team that includes full-time and part-time clinical research coordinators, research assistants, data management staff, and regulatory staff providing flexible and corporate support.
Heart Institute - Clinical Research Associate I, Susan Cheng Team Cedars-Sinai Medical CenterHeart Institute - Clinical Research Associate I, Susan Cheng TeamLos Angeles, CAAssists with regulatory submissions to the Institutional Review Board (IRB) and works closely with supervising research staff or directly with the Institutional Review Board to submit Adverse Events, Serious Adverse Events, and Safety Letters in accordance with local and federal guidelines. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.
Clinical Research Associate I - Heart Institute - Bairey-Merz Lab Cedars-Sinai Medical CenterClinical Research Associate I - Heart Institute - Bairey-Merz LabLos Angeles, CAFrom genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes. The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving patients access to the highest level of care.
Clinical Research Associate I - Heart Institute - Berman Lab Cedars-Sinai Medical CenterClinical Research Associate I - Heart Institute - Berman LabBeverly Hills, CAThe Smidt Heart Institute reflects Cedars-Sinais steadfast dedication to heart disease and research innovation giving patients access to the highest level of care. From genetic counseling and targeted drug therapies to a growing array of minimally invasive procedures, Cedars-Sinai continues to stand at the forefront of technology, innovation and discovery improving patient outcomes.
Assistant Clinical Research Coordinator - Pediatrics University of CaliforniaAssistant Clinical Research Coordinator - PediatricsLos Angeles, CA$30.74–$49.46 / hourHSR faculty conduct research with systems-level impact on child health in areas including childhood adversity, children with medical complexity, early childhood development, education and school systems, housing and health, obesity prevention, poverty, primary care and healthcare systems, vaccine delivery and uptake, and youth incarceration. The AMP ACEs project is a community-based research initiative designed to evaluate whether a telephone-based Adverse Childhood Experiences (ACEs) screening and care coordination model delivered through 211LA increases referrals to, and receipt of, ACEs-related services.
Clinical Research Regulatory Specialist University of Southern CaliforniaClinical Research Regulatory SpecialistLos Angeles, CA$75,968.95–$81,000 / yearWhen extending an offer of employment, the University of Southern California considers factors such as, but not limited to, the scope and responsibilities of the position, the candidate's work experience, education/training, key skills, internal peer equity, federal, state and local laws, contractual stipulations, grant funding, as well as external market and organizational considerations. JOB ACCOUNTABILITIES: Learns and masters the creation, initiation, development, and revision of protocols, informed consents, case report forms, and other study and clinical research documentation to support principal investigators and quality assurance systems for the Clinical Investigations Support Office.
Clinical Research Associate II Jordi Labs LLCClinical Research Associate IICAOur tailored solutions deliver regulatory and quality expertise, FDA-recognized laboratory services, clinical trials, and reimbursement strategies across device types and therapeutic areas to bring life-changing technologies to patients - faster, safer, better. Behaviors: Action-Oriented, Approachability, Building Effective Teams, Business Acumen, Career Ambition, Composure, Courage (Managerial), Customer Focus, Decision Quality, Informing, Integrity & Trust, Interpersonal Savvy, Planning.
Product Manager - BrainWatch Clinical & Evidence Strategy Natus Medical IncProduct Manager - BrainWatch Clinical & Evidence StrategyCA$90,000–$100,000 / yearFOR MORE THAN 80 YEARS, Natus has been working in collaboration with clinicians to deliver industry-leading neuro solutions that help providers more easily make sense of the body's signals. The role ultimately owns clinical product-market fit, ensuring BrainWatch is clinically validated, workflow-aligned, and evidence-backed to support adoption and differentiation.