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
Vacancy posted 5 days ago
Similar jobs that could be interesting for youBased on the Clinical Research Associate I: Data, IRB & Study Coordination in Los Angeles, CA vacancy
- ...join a dynamic research team at Cedars-Sinai... .... The Clinical Research Associate I will work both... ...to support the coordination and execution of... ...-based research studies. This role is ideal... ...managing study data, ensuring compliance... ...Review Board (IRB), including Adverse...DataDaily paidLocal areaRemote work
Cedars-Sinai
Los Angeles, CA7 days ago - ...contributor to serve as a CLINICAL RESEARCH ASSOCIATE II to Dr. Judy... ...a Clinical Research Coordinator, Research Program... ...increasingly complex research studies. Supports objectives... ...tasks such as data collection, prescreening... ..., assisting in IRB submission activities...DataLocal areaRemote work
Cedars-Sinai
Los Angeles, CA5 days ago - Cedars-Sinai is seeking a Clinical Research Associate II who will work independently to coordinate and implement complex research studies at the Smidt Heart... ...collecting clinical research data, prescreening participants, and assisting with IRB submissions while ensuring...Data
- ...Job Title Clinical Research Associate I Job Description The... ...a Clinical Research Coordinator, Research Program Administrator... ...and/or implement the study. This role evaluates... ...abstracts research data and ensures... ...regulatory submissions to the IRB. Provides limited...DataWork at officeLocal 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 areaShift work
- The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research... ...and/or implement the study. Evaluates and abstracts research data and ensures compliance... ...regulatory submissions to the IRB. Provides limited...DataLocal area
- ...scientists and researchers who are making... ...most advanced clinical trials in the world... ...Research Associate I opportunity to... ...patients. Dr. Tan’s studies on brain aging... ...Research Coordinator, Research Program... ...abstracts research data and ensures... ...submissions to the IRB. Provides...DataLocal area
- ...cancer care through data‑driven innovation. Our research brings together clinical, genomic, imaging... ...Research Associate, you will have the... ...Clinical Research Coordinator, Research Program... ...noncomplex research studies. Supports objectives... ..., assisting in IRB submission...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
- ...groundbreaking biomedical research facilities and... ...of care. The Clinical Research Associate II works... ...Clinical Research Coordinator, Research Program... ...complex research studies. Supports objectives... ...complex tasks such as data collection,... ...participants, assisting in IRB submission...DataLocal 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... ...verification against case report form data, including informing the site staff of any entry...DataFull timeContract workTemporary workWork at officeLocal areaImmediate startRemote workWork from homeHome officeFlexible hoursMedpace
Los Angeles, CA1 day ago- ...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
Los Angeles, CA3 days ago - 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
- Itlearn360 is looking for a Clinical Research Associate I in Los Angeles, CA, to assist in coordinating and implementing clinical studies. The role involves evaluating research data, ensuring protocol compliance, and completing case report forms. Candidates should have...Data
- A leading healthcare provider in Los Angeles seeks a Clinical Research Associate I/CPT to assist in coordinating noncomplex clinical research studies. Responsibilities include data collection, participant scheduling, and maintaining compliance with regulatory standards....Data
- ...Sinai Medical Center in Los Angeles is looking for a Clinical Research Associate I to manage and implement clinical research studies. You will evaluate research data, assist with regulatory submissions, and coordinate patient visits. An ideal candidate has a Bachelor's...DataLocal area
- ...Part Time Clinical Research Assistant The Research Assistant... ...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. Angel City...DataContract workPart timeLive inWork at office
- Cedars-Sinai is seeking a Clinical Research Associate I to join Dr. Zaldy Tan's team in Los Angeles. In this role, you'll coordinate research studies, evaluate clinical data, and ensure compliance with all regulatory guidelines. The position follows a hybrid schedule, allowing...DataPart timeRemote work
$22 - $30 per hour
Clinical Research Assistant in Los Angeles, CA (9006... ...supports the planning, coordination, and execution of... ...research studies under the direct... ...ensure accurate data collection and regulatory... ...Review Board (IRB) requirements,... ...Qualifications Education: Associate degree in a...DataWork at officeMonday to FridayFlexible hours$140k - $165k
...Senior Clinical Research Associate - Remote Position The Senior Clinical Research Associate (Sr... ...to questions, resolve issues (eg, data queries, study management), support the site staff... ...health-related experience (eg, study coordinator, research lab, pharmaceutical/...DataRemote jobFull timeInterim roleWork at officeWork from homeHome officeMonday to FridayNight shiftWeekend workAfternoon shift- 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$28.69 - $34.21 per hour
UCLA Outpatient Clinics seeks a full-time Neurocognitive Assessment Coordinator to support clinical research at the Semel Institute for Neuroscience... ...assessments, managing data, and collaborating with research... ...and contributing to studies focused on serious mental illnesses...DataFull time- ...Direct Jobs in Los Angeles is looking for a Clinical Research Coordinator. This role involves coordinating clinical research studies from design through closure, ensuring compliance... ...regulatory standards, and managing patient data. Applicants should have a Bachelor's degree...Data
$65 - $90 per hour
...Overview C-Clinical is looking for an experienced Senior Clinical Research Associate to support clinical trials across the Los Angeles... ...-quality execution of complex studies. The position includes both remote... ...protocol compliance. Maintain data integrity and regulatory...DataHourly payRemote workC-Clinical
Los Angeles, CA1 day ago$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - Southern California ICON plc is a world-leading healthcare... ...'s Oncology clinical trials to ensure data integrity, subject safety, and... ...with local Institutional Review Board (IRB)/Ethics Committee (EC) submissions and...DataWork experience placementInterim roleLocal areaRemote workFlexible hoursICON plc
Los Angeles, CA3 days ago$71.9k - $189k
...ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol,... ...with contracted scope of work and Good Clinical Practice. • Work with sites to... ...skill in applying, applicable clinical research regulatory requirements. • i.e.,...DataFull timePart timeLocal areaImmediate startWorldwideIQVIA
West Hollywood, CA4 days ago- Angel City VA is seeking a part-time Clinical Research Assistant in Los Angeles to support Clinical Research Coordinators in achieving study goals. The role demands creating patient charts... ...study supplies, and handling data entry. Candidates should have strong computer...DataPart time
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Clinical Research Associate I: Data, IRB & Study Coordination. Be the first to apply!
Related searches
- clinical research administrator Los Angeles, CA
- clinical research associate Los Angeles, CA
- clinical research assistant Los Angeles, CA
- on-site clinical research associate (traveling/remote) Los Angeles, CA
- senior clinical research associate Los Angeles, CA
- clinical trials assistant Los Angeles, CA
- data Los Angeles, CA
- data collection researcher Los Angeles, CA
- data reviewer Los Angeles, CA
- data technician Los Angeles, CA