Alzheimer’s Clinical Research Associate I - Data & Trials
Jobtailor
Jobtailor is seeking a Clinical Research Data Coordinator to collect, evaluate and abstract clinical research data, and to enter and process data into sponsor-provided EDC systems. You will also complete Case Report Forms and help schedule visits, supporting long-term follow-up. Responsibilities include regulatory submissions to IRB, preparing safety communications, assisting with budgets and billing, sample preparation and logistics, and ensuring compliance with FDA, HIPAA, GCP and study #J-18808-Ljbffr Jobtailor
- Responsibilities Collects, evaluates and/or abstracts clinical research data. May assist in designing forms for data collection/abstraction. Enters... ...with local and federal guidelines. Assists with clinical trial budgets and patient research billing. Responsible for sample...DataLocal area
- ICON Strategic Solutions in Los Angeles is seeking a Clinical Research Associate to conduct site qualification, initiation, monitoring, and close-out visits for clinical trials. You will ensure protocol compliance, data integrity, and patient safety throughout the trial...Data
$35 - $50 per hour
...As a Clinical Trial Assistant, you will support a single molecule across... ...Management Systems (CTMS) data that is in place but not yet... ...with internal teams, Contract Research Organizations (CROs), and... ...side CTA or Clinical Research Associate (CRA) experience. Strong...DataContract workTemporary workRemote workFlexible hours1 day per week- 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. Responsibilities include evaluating research data, entering data into electronic systems, and assisting with...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
- Cedars-Sinai in Los Angeles is seeking a Clinical Research Associate to join the Dou Lab, contributing to data-driven cancer care innovation. In this role, you will collaborate with leading scientists, gain hands-on experience with advanced computational methods, and perform...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
$110.52k - $138.15k
Senior Clinical Research Associate - Oncology - Southern CaliforniaICON is a global healthcare intelligence... ...activities throughout the clinical trial lifecycle. This Sr. CRA role will support... ...'s Oncology clinical trials to ensure data integrity, subject safety, and...DataFull timeInterim roleLocal areaRemote work- ...transforming cancer care through data-driven innovation. Our research brings together clinical, genomic, imaging, and... ...making. As a Clinical Research Associate, you will have the opportunity... ...participants for various clinical trials. Schedules research participants...DataLocal area
- ...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... ...participants for various clinical trials. Schedules research participants for...DataLocal areaRemote work
$71.9k - $189k
...study(ies) and reporting study data as required by the study... ...contracted scope of work and Good Clinical Practice. • Work with sites... ...are available for filing in the Trial Master File (TMF) and verify that... ...applying, applicable clinical research regulatory requirements. • i...DataFull timePart timeLocal areaImmediate startWorldwide$91.34k - $114.17k
...Clinical Research Associate - Early Stage Development - West Region ICON plc is a world-leading healthcare intelligence and... ...II at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments...DataWork experience placementRemote workFlexible hours- ...groundbreaking biomedical research facilities and world-class... ...doing in this role? The Clinical Research Associate I works directly with a Clinical... ...and abstracts research data and ensures compliance with... .... Assists with clinical trial budgets. Assists with patient...DataLocal area
$96.2k - $151.4k
...throughout all phases of a clinical research study, taking overall responsibility... ...through all phases of the trial. Performs clinical study... ..., Site Monitoring Plan and associated documents. Gains an in-... ...various tools to ensure: Data generated at site are complete...DataFor contractorsLocal areaRemote work2 days per week3 days per week- ...leading healthcare institution in Beverly Hills is looking for a Clinical Research Coordinator to manage research projects and maintain... ...protocols, developing budgets, and ensuring funding throughout trials. This role offers a chance to work with a diverse team committed...
- ...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... ...to develop and maintain trial management systems. Ensures compliance...DataLocal areaRemote work1 day per week
- ...The Clinical Research Associate I works under the direction of a Clinical Research Coordinator, Research... ...studies through noncomplex tasks such as data collection, prescreening of potential... ...participants for various clinical trials. Schedules research participants for research...DataDaily paidFull timeLocal area
$60k - $140k
Job SummaryClinical Research Coordinators wanted at Medpace... ...-based opportunity for clinical research professionals... ...fill Clinical Research Associate (CRA) openings with... ...against case report form data, including informing... ...our integrated Clinical Trial Management System to identify...DataFull timeContract workTemporary workWork at officeRemote workWork from homeFlexible hours- ...dedication to heart disease and research innovation giving patients... ...! Job Summary: The Clinical Research Associate I works directly with a... ...evaluates and abstracts research data and ensures compliance with... .... Assists with clinical trial budgets and patient...DataFull timeWork at officeLocal area
$140k - $165k
...Primary Objective of Position The Senior Clinical Research Associate (Sr. CRA) is responsible for acting as... ...sites for all assigned clinical trial-related activities, to ensure trials are... ...to questions, resolve issues (eg, data queries, study management), support the...DataFull timeInterim roleWork at officeRemote workWork from homeHome officeMonday to FridayNight shiftWeekend workAfternoon shift$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 is well-suited for professionals... ...and protocol compliance. Maintain data integrity and regulatory compliance...DataHourly payRemote work- The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program... ...study. Evaluates and abstracts research data and ensures compliance with protocol... ...federal guidelines. Assists with clinical trial budgets. Assists with patient...DataLocal area
$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- ...alongside physician-scientists and researchers who are making life-saving... ...some of the most advanced clinical trials in the world. The Pulmonary... ...Role The Clinical Research Associate I will work under the... ...through noncomplex tasks such as data collection, prescreening of...DataLocal area
- ...Pramod Butte, Ph.D. is looking for a Clinical Research Associate I to join a diverse team! The primary... ...will assist in validating the clinical trial of groundbreaking medical imaging systems... ...clinical trials, collecting clinical data, and play a crucial part in developing...DataDaily paidLocal areaImmediate start
$19.5 - $32.86 per hour
Clinical Research Associate I - Department of Medicine Join to apply for the Clinical Research Associate... ...studies through noncomplex tasks such as data collection, prescreening of and... ...federal guidelines. Assists with clinical trial budgets and patient research billing....DataDaily paidFull timeLocal areaWork from homeShift work$110.52k - $138.15k
Senior Clinical Research Associate - Oncology - West Region ICON plc is a world-leading healthcare intelligence... ..., return, or destruction Resolve data queries and drive timely, high-quality... ...Cancer) and/or Hematology Oncology trials Proficient in ICH‑GCP, local...DataWork experience placementLocal areaVisa sponsorshipFlexible hours- Irvine Clinical Research - West Los Angeles / Inglewood location seeks a Clinical Research Coordinator I to manage day-to-day trial operations, coordinate visits, and ensure data integrity under GCP standards. You will work closely with Principal Investigators and our clinical...DataFull time
- ...please visit: . About the Role The Clinical Research Coordinator I works independently... ...protocol eligibility, presenting non-medical trial concepts and details, and participating... ...for accurate and timely source documents, data collection, documentation, entry, and...DataFull timeLocal area
$91.34k - $114.17k
Clinical Research Associate - Oncology - West RegionICON is a global healthcare intelligence and clinical research organisation united by a mission... ...and ensure proper storage, return, or destructionResolve data queries and drive timely, high-quality data entryDocument site...DataFull timeLocal area
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