- Cedars-Sinai (Los Angeles, CA)
- …Safety Letters in accordance with local and federal guidelines. *Assists with clinical trial budgets. *Assists with patient research billing. *Schedules patients ... Clinical Research Associate I (CRAI) will work directly with a Clinical Research Coordinator , Research Program Administrator, Research Nurse, or Principal… more
- Cedars-Sinai (Los Angeles, CA)
- …and Safety Letters in accordance with local and federal guidelines. + Assists with clinical trial budgets. + Assists with patient research billing. + Schedules ... Clinical Research Associate I works directly with a Clinical Research Coordinator , Research Program Administrator, or...research data from source documents. + Ensures compliance with protocol and overall clinical research objectives. +… more
- Cedars-Sinai (Los Angeles, CA)
- …and Safety Letters in accordance with local and federal guidelines *Assists with clinical trial budgets. *Schedules research participants for research visits and ... The Clinical Research Associate II works directly with a Clinical Research Coordinator , Research Program Administrator, or Research Nurse, or… more
- Cedars-Sinai (Los Angeles, CA)
- …Safety Letters in accordance with local and federal guidelines. *Assists with clinical trial budgets. *Assists with patient research billing. *Schedules patients ... The Clinical Research Associate I works directly with a Clinical Research Coordinator , Research Program Administrator, or Research Nurse to… more
- Cedars-Sinai (Los Angeles, CA)
- …and Safety Letters in accordance with local and federal guidelines. + Assists with clinical trial budgets. + Assists with patient research billing. + Schedules ... Clinical Research Associate I works directly with a Clinical Research Coordinator , Research Program Administrator, or...research data from source documents. + Ensures compliance with protocol and overall clinical research objectives. +… more
- J&J Family of Companies (Danvers, MA)
- …software or product testing, and site closeouts. As a subject matter expert on clinical trial protocol and technologies, the Field Research Specialist acts ... related enrollment and procedures. + Serve as a technology, protocol and clinical trial procedure...with key site personnel including the Principal Investigator, Research Coordinator , as well as regulatory and legal personnel. +… more
- University of Colorado (Aurora, CO)
- …assessments and conduct study interviews. + Responsible for data management for all clinical trial data. Collect, code, and analyze data obtained from research ... ** Clinical Research Professional** **Description** **University of Colorado Anschutz...**Job Summary:** Key Responsibilities: + Act as a Primary Coordinator on multiple trials/studies, managing the day-to-day operations. +… more
- University of Southern California (Los Angeles, CA)
- … clinical assessments that are required per the clinical trial protocol in close coordination with the study coordinator and other team members as ... studies and interprets finished results. + Contributes to the implementation of specific clinical trial protocols and the clinical management of patients on … more
- Cedars-Sinai (Los Angeles, CA)
- …Associate at Cedars-Sinai, you will assist in the effort in validating the clinical trial of groundbreaking medical imaging systems. The job will provide ... The CRA I member will work directly with a Clinical Research Coordinator , Research Program Administrator, or...handle, and process fresh and fixated specimens per outlined protocol Perform scanning of specimens using clinical … more
- Pfizer (New Haven, CT)
- …of a study - Answers and resolves any query sent by project manager or clinical coordinator BASIC QUALIFICATIONS - Minimum of a bachelor's degree in nursing or ... for data and sample collection and safety of the trial subjects. This individual focuses on the clinical...and Pfizer SOPs - Executes and is responsible for protocol required data and sample collection in accordance with… more
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