The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on each study ...
Accountant, Accounting Clerk, Accounts Payable Specialist, Accounts Payable Administrator, Accounts Payable Manager, Billing and Collections Analyst, Billing and Collections Coordinator, Billing and Collections Manager, Bookkeeper, Chief Financial Officer, Controller, Comptroller, Credit Analyst, Fi...
The Clinical Research Coordinator II (CRC II) is the backbone of our clinical research operations, overseeing the day-to-day execution of multiple complex trials across various therapeutic areas and research phases. Clinical Research Coordinator II. Become a Clinical Research Expert:. Provide suppor...
Accountant, Accounting Clerk, Accounts Payable Specialist, Accounts Payable Administrator, Accounts Payable Manager, Billing and Collections Analyst, Billing and Collections Coordinator, Billing and Collections Manager, Bookkeeper, Chief Financial Officer, Controller, Comptroller, Credit Analyst, Fi...
Act as a floating Clinical Research Coordinator to coordinate the daily aspects of multiple ophthalmic clinical trials, as assigned. Prepare documents for submission to the Office for Protection of Research Subjects. Create, organize, and maintain files, records and reports on all research subjects....
Accountant, Accounting Clerk, Accounts Payable Specialist, Accounts Payable Administrator, Accounts Payable Manager, Billing and Collections Analyst, Billing and Collections Coordinator, Billing and Collections Manager, Bookkeeper, Chief Financial Officer, Controller, Comptroller, Credit Analyst, Fi...
Join as a Clinical Research Coordinator, managing pivotal phases of clinical research activities from design to closeout. Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the prep...
The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. Responsible for compiling and reporting on e...
The Clinical Research Coordinator contributes to the overall. The Clinical Research Coordinator. Practice (GC) for clinical research. ...
The Clinical Research Coordinator I assists pediatric psychologist and physician scientists in the development and implementation of clinical research focusing on the immediate and long-term evaluation of integrative medicine practices on health outcomes of children with chronic/critical illness and...
The Research Administrative Coordinator works under the direction of the Research Director; Research Manager; and the Research Operations Associate of the assigned research area. Working Title** : Research Admin Coordinator - Cheng Lab, Heart Institute. The Smidt Heart Institute reflects Cedars-Sin...
The Clinical Research Coordinator III, as a certified research professional, handles clinical trial administration for all protocol phases for the Leukemia and Lymphoma Disease department. ACRP Certified Clinical Research Coordinator (CCRC) or SoCRA Certified Clinical Research Professional (CCRP). H...
The Research Administrative Coordinator works under the direction of the Research Director; Research Manager; and the Research Operations Associate of the assigned research area. Assists Senior Project Advisor with research related work, such as submitting check requests for study related expenses a...
Position Summary: The Clinical Research Coordinator II, as a certified research professional, handles clinical trial administration for all protocol phases. ACRP Certified Clinical Research Coordinator (CCRC) or SOCRA Certified Clinical Research Professional (CCRP). Here world-class experts in medic...
Join our team and use your skill with an organization known nationally for excellence in research! Job Summary: The Research Administrative Coordinator works under the direction of the Research Director; Research Manager; and the Research Operations Associate of the assigned research area. Req ID : ...
We are looking for a passionate and dedicated Clinical Research Coordinator II to join our team. The Clinical Research Coordinator II works independently providing study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details...
Overview Position Summary: The Clinical Research Coordinator III, as a certified research professional, handles clinical trial administration for all protocol phases. ACRP Certified Clinical Research Coordinator (CCRC) or SoCRA Certified Clinical Research Professional (CCRP) required. Here world-cla...
Screening and recruitment of potential patients for protocol eligibility.Scheduling patients and maintain consent forms and case reports.Data collection and reporting for sponsors and regulatory bodies.Coordinate internal and external audits.Submit adverse events, protocol deviations, and safety let...
Prepare and process all Institutional Review Board (IRB)through the IRB and other regulatory groups as apropriate including initial submissions, amendments, continuing reviews, adverse events and serious adverse events.Coordinate, organize and maintain all documentation required by sponsor or CRO (c...
The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process. The Smidt Heart Institute reflects Cedars-Sinai's stea...
The Senior Clinical Research Coordinator plays a critical role in the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The ideal candidate is an experienced professional or leader who has direct responsibility for the implemen...
Coordinate and conduct clinical studies, includes; subject recruitment, informed consent, chart maintenance and data entry.Coordinate IRB submissions and renewals in accordance with FDA and IRB guidelines.Assure compliance with the protocol and regulatory requirements includes: collecting, recording...
We’re seeking a self-motivated, independent professional with: * Knowledge of health services or clinical research methodology and principles * Computer proficiency with Microsoft Word/Excel/Publisher/Access * In-depth understanding of Human Subject Protection and informed consent * Experience follo...
The Research Administrative Coordinator works under the direction of the Research Director; Research Manager; and the Research Operations Associate of the assigned research area. The Smidt Heart Institute reflects Cedars-Sinai's steadfast dedication to heart disease and research innovation giving pa...
With minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple human subjects’ (clinical) research projects and is expected to perform all core Clinical Research Coordinator (CRC) responsibilities. Association of Clinical Research...