Clinical Research Associate I: Data, IRB & Study Coordination
Women Veterans Interactive
Women Veterans Interactive is looking for a Clinical Research Associate I in Los Angeles, California. The role involves assisting in the coordination and implementation of research studies, including data collection and compliance with federal guidelines. Candidates should possess a High School Diploma/GED, with a Bachelor's Degree preferred, and ideally have clinical research experience. The position emphasizes strict adherence to patient confidentiality and regulatory standards, offering exposure to varied clinical research tasks. #J-18808-Ljbffr Women Veterans Interactive
- Cedars-Sinai Medical Center is seeking a Clinical Research Associate I in Los Angeles, CA. This role involves coordinating clinical studies, evaluating research data, ensuring compliance with regulations, and managing patient contact under supervision. Candidates should...Data
- Cedars-Sinai in Los Angeles is looking for a Clinical Research Associate I to join their team. This role involves aiding in the coordination and implementation of noncomplex research studies and supporting the objectives through data collection and participant scheduling....Data
- ...commutable area. The Clinical Research Associate II works... ...a Clinical Research Coordinator, Research Program Administrator... ...increasingly complex research studies. Supports objectives... ...tasks such as data collection, prescreening... ..., assisting in IRB submission activities...DataLocal area
- ...for excellence in research! Joseph Schwab... ...Medical Center The Clinical Research Associate I works under the... ...Research Coordinator, Research Program... ...noncomplex research studies. Supports objectives... ...tasks such as data collection, prescreening... ..., assisting in IRB submission...DataDaily paidLocal area
- ...groundbreaking biomedical research facilities and... ...this role? The Clinical Research Associate I works directly... ...Research Coordinator, Research Program... ...or implement the study. Evaluates and abstracts research data and ensures compliance... ...to the IRB. Provides limited...DataLocal area
- ...heart disease and research innovation giving... ...Summary: The Clinical Research Associate I works directly... ...Clinical Research Coordinator, Research Program... ...or implement the study. This role evaluates... ...research data and ensures compliance... ...submissions to the IRB. Provides limited...DataWork at officeLocal area
- ...groundbreaking biomedical research facilities and... ...is looking for a Clinical Research Associate II to join the... ...research studies. He has authored... ...Clinical Research Coordinator, Research Program... ...noncomplex tasks such as data collection,... ...participants, assisting in IRB submission...DataLocal area
- Cedars-Sinai Medical Center in Los Angeles is seeking a Clinical Research Associate I to join our team. The successful candidate will coordinate clinical research efforts, maintain compliance with regulatory guidelines, and assist with patient contact as necessary. A High...
- ...join a dynamic research team at Cedars-Sinai... .... The Clinical Research Associate I will work both... ...to support the coordination and implementation... ...community-based studies. Responsibilities... ...administration, data collection and management... ...Review Board (IRB), including...DataDaily paidLocal areaRemote work
- ...opportunity! As a Clinical Research Associate I, you will work under... ...a Clinical Research Coordinator, Research Program Administrator... ...non-complex research studies. The incumbent will... ...tasks such as data collection, pre-screening... ..., assisting in IRB submission activities...DataLocal area
- ...Los Angeles is seeking a Clinical Research Associate I to support the coordination and implementation of clinical research studies. The role involves responsibilities... ...clinical research data, completing case report... ...compliance with FDA and IRB regulations. Ideal candidates...Data
- ...scientists and researchers who are making... ...most advanced clinical trials in the world... ...Research Associate I will work under... ...Clinical Research Coordinator, Research... ...noncomplex research studies. The incumbent... ...tasks such as data collection, prescreening... ..., assisting in IRB submission...DataLocal area
- ...Sinai is looking for a Clinical Research Associate II to join the... ...a Clinical Research Coordinator, Research Program Administrator... ...complex research studies. Primary Job Duties... ...abstracts clinical research data, and enters it into... ...Review Board (IRB) and may submit adverse...DataLocal area
- ....D. is looking for a Clinical Research Associate I to join a diverse team... ...collecting clinical data, and play a crucial... ...a Clinical Research Coordinator, Research Program Administrator... ...and/or implement the study. This role evaluates... ...federal, local, FDA, IRB, and HIPAA guidelines...DataDaily paidLocal areaImmediate start
- The Clinical Research Associate I works under the direction of a Clinical Research Coordinator, Research Program Administrator, Research... ...noncomplex research studies. Supports objectives... ...tasks such as data collection, prescreening... ..., assisting in IRB submission activities...DataDaily paidLocal area
$19.5 - $32.86 per hour
Clinical Research Associate I - Department of Medicine Join to apply for... ...a Clinical Research Coordinator, Research Program... ...noncomplex research studies. The incumbent will support... ...tasks such as data collection, prescreening... ...participants, assisting in IRB submission activities...DataDaily paidFull timeLocal areaWork from homeShift work$60k - $140k
...Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) (LA) Clinical Research Coordinators wanted at Medpace! Become a CRA and join our growing team... ...documentation verification against case report form data, including informing the site staff of any...DataFull timeContract workTemporary workWork at officeLocal areaImmediate startRemote workWork from homeHome officeFlexible hours- ...Cedars-Sinai! The Angeles Clinic & Research Institute has established an... ...research! The Clinical Research Data Associate II manages the data for assigned research studies. This will include, designing... ...Key Responsibilities: Coordinates data for research studies....DataLocal area
- Cedars-Sinai is seeking a Clinical Research Associate I to work with research teams at the Smidt Heart Institute. This position involves coordinating clinical studies, evaluating data, and ensuring compliance with research protocols. Applicants should have at least a high...Data
- Cedars-Sinai is seeking a Clinical Research Associate II to join the Smidt Heart Institute, collaborating with a team to coordinate complex research studies. This role requires a High School Diploma... ...research, evaluating clinical data, and ensuring protocol compliance...Data
- Cedars-Sinai Medical Center is seeking a Clinical Research Associate I for the CSF Leak Research Program in the Department of Neurology. The role requires assistance in coordinating noncomplex research studies through data collection and participant scheduling. The ideal...Data
- Cedars-Sinai is looking for a Clinical Research Associate I in Los Angeles, California. This role involves assisting in the coordination and implementation of noncomplex research studies, collecting and processing clinical research data, and prescreening research participants...Data
$45k - $66k
...- $66,000.00/yr Clinical Research Assistant in Los... ...supports the planning, coordination, and execution of... ...research studies under the direct... ...ensure accurate data collection and regulatory... ...Review Board (IRB) requirements, and... ...Qualifications: Education: Associate degree in a...DataWork at officeMonday to FridayFlexible hours- Title: Part time Clinical Research Assistant Job Summary: The... ...support to Clinical Research Coordinators in the completion of protocol-specific study goals while observing... ...Timely completion of data entry and query... ...regulations (GCP, FDA, IRB) is a plus Seniority level...DataContract workPart timeWork at office
- Clinical Research Assistant (Must Live in Los Angeles... ...Research Coordinators in the completion... ...protocol-specific study goals while observing... ...Timely completion of data entry and query... ...regulations (GCP, FDA, IRB) is a plus... ...Research Research Associate I - Heart Institute...DataFull timeContract workPart timeLive inWork at officeWork from home
- Clinical Research Associate II job at Ellison Institute, LLC. Los Angeles, CA. Job... ...integrate the interdisciplinary study and treatment of disease. We... ...of critical biospecimen data and compliance with research... ...institutional review boards (IRBs) and regulatory agencies. Assist...Data
$20 - $32 per hour
Overview Flourish Research is looking for motivated... ...actively hiring Clinical Research... ...clinical research studies under the supervision... ...Clinical Research Coordinator. This role assists... ...ensuring accurate data collection and compliance with GCP, IRB, and sponsor protocols...DataWork at officeMonday to FridayShift work$36.9 - $41.03 per hour
...Southern California is seeking a detail-oriented Research Coordinator II for their Department of Population and... ...Sciences. The role involves coordinating study activities, maintaining participant communication, and managing data for NIH-funded research grants. The ideal...DataHourly payFlexible hours- Come join our team! The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program... ...and/or implement the study. Evaluates and abstracts research data and ensures compliance... ...regulatory submissions to the IRB. Provides limited...DataDaily paidLocal area
- Clinical Research Associate ICON plc is a world-leading healthcare intelligence and clinical research... ...trials, interpreting complex medical data, and contributing to the advancement of... ...investigators and site staff to facilitate smooth study conduct. ~ Performing data review...DataFlexible hours
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