Clinical Research Coordinator II Translational Trials

Vanderbilt Health

Nashville (TN)

In loco

USD 55.000 - 85.000

Tempo pieno

3 giorni fa

Candidati tra i primi

Una candidatura completa in un minuto

Curriculum e lettera di presentazione personalizzati, pronti da inviare.

Supera i filtri ATS

Descrizione del lavoro

The Clinical/Translational Research Coordinator II at Vanderbilt Health coordinates the approval processes and conduct of research protocols, ensuring integrity and quality in compliance with policies and regulations.

This role involves preparing IRB submissions, maintaining regulatory documents, coordinating site visits, supporting participant screening, recruitment, and data collection across trials within our academic medical center, and contributing to regulatory compliance and study

Competenze

Coordinate IRB submissions, amendments and continuing review applications per policies and federal regulations.
Maintain internal and sponsor-required documents for regulatory authorities and trial conduct.
Identify and procure equipment and supplies needed for trials across sites.

Mansioni

Prepare and process IRB proposals, amendments and adverse event reports.
Maintain and organize documents for regulatory authorities and sponsors.
Identify equipment and supplies needed for trials and site logistics.
Screen and recruit eligible participants and ensure ongoing eligibility across studies.
Record data from source documents onto case report forms with accuracy and timeliness.
Package and ship study specimens following sponsor requirements and regulations.