Clinical Research Associate, Data & Study Operations
UCLA Health
UCLA Health in Los Angeles is seeking a Staff Research Associate to support clinical research studies focused on gastroenterology and related conditions. You will collect and manage research data, maintain study databases, and prepare reports under the PI and senior staff. The role involves maintaining HIPAA and IRB compliance, documenting results, and supporting study operations in a collaborative team environment. This is a limited position, with potential conversion to a career role. #J-18808-Ljbffr UCLA Health
- ...Diseases at UCLA is seeking a Staff Research Associate to support clinical studies in general gastroenterology, GI hemorrhage... ...will collect and manage research data, maintain study databases, prepare reports, and assist study operations while ensuring HIPAA, IRB, and...OperationsData
$96.2k - $151.4k
...ensures compliance of study conduct with ICH/GCP... ...throughout all phases of a clinical research study, taking overall... ...Monitoring Plan and associated documents.Gains an in... ...tools to ensure: Data generated at site are... ...with GCTO country operations, finance, regulatory...OperationsDataFull timeFor contractorsLocal areaRemote workFlexible hours2 days per week3 days per week$140k - $165k
...Objective of Position The Senior Clinical Research Associate (Sr. CRA) is responsible for acting... ...(GCP) guidelines and the standard operating procedures (SOPs) in effect. Major... ...to questions, resolve issues (eg, data queries, study management), support the site staff...OperationsDataFull timeInterim roleWork at officeRemote workWork from homeHome officeMonday to FridayNight shiftWeekend workAfternoon shift$99.1k - $141.89k
The Clinical Investigations Support Office provides support... ...managing prescreening operations, assessing patient... ...coordination with the clinical research coordinators who take... ...of various research study guidelines that include... ...analyze and evaluate data, and present findings.Excellent...OperationsDataFull timeWork experience placementWork at officeLocal areaFlexible hours- SQRL is seeking a Clinical Research Assistant to support studies and clinic operations across phases I-IV, with a focus on oncology trials at our Century City site. You will help with patient visits, data collection, consent, and adherence to GCP, IRB, and sponsor protocols...OperationsData
- ...match! Focus on Oncology Research Trials! Our Client:... .... Their sites conduct studies spanning Phases I-IV and... .... The Role: The Clinical Research Assistant supports... ...assists with clinic operations and study procedures across... ..., ensuring accurate data collection and...OperationsDataCasual work
$20 - $32 per hour
Overview Flourish Research is looking for motivated,... ...We are actively hiring Clinical Research Assistants at... ...supports clinical research studies under the supervision... ...assists with clinic operations and study procedures... ...research, ensuring accurate data collection and...OperationsDataWork at officeMonday to FridayShift work- ...healthcare intelligence and clinical research organization. We’re... ...ensure adherence to study protocols, regulatory... ...ensure timely and accurate data collection and... ...facilitate smooth trial operations. Your Profile:... ...as a Clinical Research Associate, with a strong understanding...OperationsDataRemote jobWork from homeFlexible hours
- ...Can you turn that into a study we can actually sell... ...designs and runs diagnostic clinical studies. Many of the... ...work out how it should operate, build the economics,... ...Operations, laboratory, data, regulatory, and finance... ..., diagnostics, research sites, consulting, or another...OperationsDataWork at officeRelocation package
- ...Cedars-Sinai is hiring a Clinical Research Associate I to work in the Smidt Heart Institute. This role involves coordinating studies with a Clinical Research Coordinator and ensuring compliance... ...include evaluating research data, entering data into electronic systems,...Data
- ...Role Can you take a difficult clinical study, figure out what is actually... ...We need another load-bearing operator to own Clinical Operations... ...recruitment, monitoring, samples, data, and closeout. Build... ...Looking For You have run clinical research yourself. You know what...OperationsDataWork at officeRelocation package
- ...access to groundbreaking biomedical research facilities and world-class... ...you be doing in this role? The Clinical Research Associate I works directly with a... ...coordinate and/or implement the study. Evaluates and abstracts research data and ensures compliance with protocol...DataLocal area
- ...Clinical Research Associate To be eligible for this position, you must reside in the same country where the job is located. Perform... ...work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations...DataLocal area
$70 - $75 per hour
...Sr. Field Clinical Research Associate Remote with Travel required in the North Central Region (ideally... ...be responsible for monitoring clinical studies at assigned sites to ensure compliance... ...initiation, periodic and close-out visits, data and documentation review, adverse...DataHourly payContract workPart timeLocal areaRemote work$91.34k - $114.17k
...Clinical Research Associate - Early Stage Development - West Region ICON plc is a world-leading healthcare... ...trials, interpreting complex medical data, and contribute to the advancement of... ...and site staff to facilitate smooth study conduct. Performing data review and...DataWork experience placementRemote workFlexible hours- ...Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health is... ...patient's safety and clinical data integrity at an... ...effective conduct of the clinical study data review and capture. Verifies... ...each country in which it operates, including the...DataContract workInterim roleLocal areaImmediate startRemote workFlexible hours
- A prominent research organization in Los Angeles is looking for Clinical Research Assistants to contribute to life-changing research... ...involves supporting clinical operations, ensuring compliance with protocols, and collecting accurate data while providing an excellent...OperationsData
- ICON Strategic Solutions is seeking a Clinical Research Associate to support sponsor-driven trials globally. You will conduct site qualification... ...and site staff is essential to facilitate smooth study conduct, data review, and query resolution. You will also contribute...Data
- 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
- ...Sinai's Smidt Heart Institute in Los Angeles invites applications for a Clinical Research Associate I/CPT. You will assist in coordinating noncomplex research studies under supervision, supporting data collection, regulatory submissions, budgeting, and study logistics....Data
- Cedars-Sinai is seeking a Clinical Research Associate I to support coordination and implementation of noncomplex research studies. You will assist in data collection, prescreening and scheduling, and help with IRB submissions and budgeting under supervision. The role involves...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... ...compliance. Maintain data integrity and regulatory compliance...DataHourly payRemote work- Medasource is seeking a Sr. Field Clinical Research Associate for a remote, travel-based, part-time 12-month... ...to ensure GCP compliance and study protocols across sites. The candidate... ...be proficient in coordinating visits, data review, and inter-team collaboration....DataRemote jobContract workPart time
$80k - $130k
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 RDI runs sample collection studies...Data- Cedars-Sinai Medical Center is seeking a Clinical Research Associate I to work with the study team to coordinate and implement research projects. You will evaluate data from source documents, enter data into electronic systems, and assist with regulatory submissions to...Data
- ...to heart disease and research innovation giving patients... ...Job Summary: The Clinical Research Associate I works directly with... ...and/or implement the study. This role evaluates... ...abstracts research data and ensures... ...documents. Able to operate standard office equipment...DataFull timeWork at officeLocal area
- ...Clinical Research Associate The Clinical Research Associate (CRA) is responsible for establishing and maintaining the Study Master File, tracks critical trial information, and supports Regional... ...) is responsible for maintaining data integrity and monitoring study conduct...DataWork experience placementInterim roleWork at officeRemote workNight shift
- ...contributor to serve as a CLINICAL RESEARCH ASSOCIATE II to Dr. Judy Tan to support... ...complex research studies. Supports objectives of research... ...through noncomplex tasks such as data collection, prescreening of... ...such as auditing, Standard Operating Procedure development, etc....DataFull timeLocal areaRemote work
- ...physician-scientists and researchers who are making life-... ...of the most advanced clinical trials in the world.... ...The Clinical Research Associate I will work under the... ...of noncomplex research studies. The incumbent will support... ...tasks such as data collection, prescreening...DataFull timeLocal area
$91.34k - $114.17k
...Clinical Research Associate - Early Stage Development - West Region ICON plc is a world-leading healthcare... ...trials, interpreting complex medical data, and contribute to the advancement of... ...and site staff to facilitate smooth study conduct. Performing data review and...DataWork experience placementFlexible hours
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