Clinical Research Associate I: Data & Compliance
Cedars-Sinai Medical Center
Cedars-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 degree in Science, Sociology or a related field, and experience in clinical research. This role involves working closely with research teams while ensuring compliance with FDA and local guidelines. The position offers valuable experience for those aiming for a career in clinical research. #J-18808-Ljbffr
- ...As a Senior Clinical Research Associate you will work on the frontline of communication with project stakeholders, ensuring timelines, targets... ...subjects’ rights, safety and well-being and quality of data compliance. You will: Conduct and report all types of onsite...DataWork visa
- ...The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse... ...the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for...DataLocal area
- ...The Clinical Research Associate I works under the direction of a Clinical Research Coordinator, Research... ...through noncomplex tasks such as data collection, prescreening of potential... ...budget and billing, and ensuring overall compliance with all federal and local guidelines...DataDaily paidLocal 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
- ...steadfast dedication to heart disease and research innovation giving patients access... ...patient outcomes. Job Summary The Clinical Research Associate I works directly with a Clinical... ...evaluates and abstracts research data and ensures compliance with protocol and research...DataWork at officeLocal area
$19.5 - $32.86 per hour
Clinical Research Associate I - Department of Medicine Join to apply for the Clinical Research Associate... ...through noncomplex tasks such as data collection, prescreening of and scheduling... ...and billing, and ensuring overall compliance with all federal and local guidelines...DataDaily paidFull timeLocal areaWork from homeShift work- ...career at Cedars‑Sinai! The Angeles Clinic & Research Institute has established an international... ...research! The Clinical Research Data Associate II manages the data for assigned research... ...trial management systems. Ensures compliance with all federal and local agencies including...DataLocal area
$22 - $30 per hour
Clinical Research Assistant in Los Angeles, CA (90067) Summary The Research Assistant... ...activities to ensure accurate data collection and regulatory compliance in accordance with Good Clinical... ...assigned. Qualifications Education: Associate degree in a science‑related field...DataWork at officeMonday to FridayFlexible hours- ...ALLIANCE CLINICAL LLC in Inglewood, CA, is seeking an Assistant Clinical Research Coordinator (ACRC) to support the planning and execution... .... The role involves ensuring compliance with protocols and protecting... ...safety while assisting in data collection and study coordination...DataFull time
$110.52k - $138.15k
...ICON in Los Angeles is seeking a Senior Clinical Research Associate specializing in Oncology. You will serve as the primary contact between investigational sites and sponsors, ensuring compliance and supporting patient safety during trials. Qualifications include a Bachelor...- ...ICON Clinical Research seeks a Senior Clinical Research Associate in Los Angeles to oversee site compliance and monitoring for Oncology trials. You will be the primary contact between investigational sites and the sponsor, ensuring regulatory adherence. Candidates should...
$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - West ICON plc is a world-leading healthcare intelligence... ..., and close‑out Ensure site compliance with ICH‑GCP, SOPs, and regulations Maintain... ...storage, return, or destruction Resolve data queries and drive timely, high‑...DataLocal areaVisa sponsorshipFlexible hours$71.9k - $189k
...conducting the study(ies) and reporting study data as required by the study protocol,... ...accordance with contracted scope of work and Good Clinical Practice. • Work with sites to adapt,... ...skill in applying, applicable clinical research regulatory requirements. • i.e., Good...DataFull timePart timeLocal areaImmediate startWorldwide- ...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
$110.52k - $138.15k
...ICON in Los Angeles is seeking a Sr Clinical Research Associate to conduct clinical trials, ensuring data integrity and patient safety. Ideal candidates will have a Bachelor's degree and a minimum of 5 years' experience in clinical trials. Offering competitive salary between...Data- ...access to groundbreaking biomedical research facilities and world-class medical... ...you be doing in this role? The Clinical Research Associate I works directly with a Clinical Research... ...Evaluates and abstracts research data and ensures compliance with protocol and research...DataLocal area
- ...Itlearn360 is seeking a Clinical Research Associate II to oversee the execution of non-therapeutic clinical research studies... ...Los Angeles, CA. The role involves ensuring compliance with study protocols, quality control of data, and collaboration with top-tier investigators...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
- ...Women Veterans Interactive is looking for a Clinical Research Associate I in Los Angeles, California. The role involves assisting in... ...coordination and implementation of research studies, including data collection and compliance with federal guidelines. Candidates should possess a...Data
$80k - $130k
...What This Is What This Is You own IVD diagnostic clinical studies end-to-end — site activation through data lock — across multiple active trials at once. You are not a monitor who writes reports. You are the person who makes studies move. The Culture The Culture RDI runs...Data- ...execution of treatment-use and clinical support activities by... ...team. Supports activities associated with out-of-specification programs... ...works with multiple contract research organizations and external partners... ...as screening, enrollment, data flow, protocol deviations,...DataContract workInterim role
$65 - $90 per hour
...Overview C-Clinical is looking for an experienced Senior Clinical Research Associate to support clinical trials across the Los Angeles region. This opportunity... ...high-quality execution and protocol compliance. Maintain data integrity and regulatory compliance throughout...DataHourly payRemote work- ...‑organized contributor to serve as a CLINICAL RESEARCH ASSOCIATE II to Dr. Judy Tan to support community... ...through noncomplex tasks such as data collection, prescreening of potential... ...budget and billing, and ensuring overall compliance with all federal and local guidelines...DataLocal areaRemote work
- ...Thecardiacsuite is seeking a Clinical Research Associate to support clinical research protocols and assist in maintaining regulatory compliance. This position involves collaboration with multidisciplinary teams, ensuring adherence to regulations during clinical trials...
$110.52k - $138.15k
...Senior Clinical Research Associate - Oncology - West ICON plc is a world-leading healthcare intelligence... ..., and close-out Ensure site compliance with ICH-GCP, SOPs, and regulations Maintain... ...storage, return, or destruction Resolve data queries and drive timely, high-...DataWork experience placementLocal areaVisa sponsorshipFlexible hours- Cedars-Sinai is hiring a Clinical Research Associate I to work in the Smidt Heart Institute. This role... ...Clinical Research Coordinator and ensuring compliance with research protocols. Ideal... ...Responsibilities include evaluating research data, entering data into electronic...Data
- Cedars-Sinai in Los Angeles is looking for a Clinical Research Associate I to join their team. This role involves... ...Coordinators to implement studies, ensuring compliance with protocols while evaluating clinical research data and assisting with regulatory submissions. The...Data
- Cedars-Sinai in Los Angeles is seeking a Clinical Research Associate I to join their innovative team. This role involves coordinating clinical studies, ensuring compliance with protocols, and managing research data. You'll support a dedicated group committed to advancing...Data
- Cedars-Sinai in Los Angeles is seeking a Clinical Research Associate I to support the coordination and implementation... ...responsibilities such as evaluating clinical research data, completing case report forms, and ensuring compliance with FDA and IRB regulations. Ideal...Data
- ...in Los Angeles invites applications for the role of Clinical Research Associate I. This position involves collaborating with a diverse... ...include patient scheduling for research visits, managing data, and ensuring compliance with relevant protocols. Join us to be part of...Data
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