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Cedars-Sinai
Overview
The Clinical Research Associate I will assist in coordinating and implementing non-complex research studies, including tasks such as data collection, scheduling participants, and ensuring compliance with guidelines. The role involves supporting supervising staff with regulatory submissions and maintaining research practices.
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Compensation
Salary not listed
Posted
22 days ago
Coordinates and implements complex clinical research studies by managing data collection, participant scheduling, and IRB submissions. Serves as a primary contact for sponsors and provides training to junior staff to ensure protocol compliance.
$24 - $36 / HOUR
25 days ago
Assist in the coordination and implementation of noncomplex research studies through data collection and participant scheduling. Support regulatory compliance by assisting with IRB submissions and maintaining GCP and HIPAA standards.
$24 - $33 / HOUR
1 month ago
The Clinical Research Associate I coordinates clinical study implementation, abstracts research data, and ensures compliance with federal and institutional regulations. They are responsible for completing case report forms, managing regulatory submissions to the IRB, and assisting with patient research billing.
The Clinical Research Associate I assists in the coordination and implementation of clinical studies, including data abstraction, entry into electronic systems, and regulatory compliance. They also support patient scheduling, sample management, and financial tasks such as trial budgets and research billing.
ALLIANCE CLINICAL LLC
Responsibilities include communicating with study participants, collecting medical histories, obtaining informed consent, and managing study drug accountability per protocol. The role also involves performing protocol-specific procedures like EKGs and phlebotomy, collecting and processing biological samples, and ensuring timely data documentation.
2 months ago
