Clinical Research Coordinator II - Translational Trials & Impact

Vanderbilt University Medical Center; United States; Sur place; USD 65 000 - 80 000; Plein temps

Résumé du poste

Vanderbilt Health in the United States seeks a Clinical/Translational Research Coordinator II to coordinate approval processes and conduct of research protocols, ensuring integrity and adherence to policies.

This role involves preparing IRB submissions, maintaining regulatory documents, participating in sponsor site visits, handling data capture, and collaborating with investigators and teams across sites to keep trials on track.

Qualifications

• Experience with clinical/translational research processes.
• Familiar with regulatory documentation and source data collection.
• Knowledge of good clinical practice standards.

Responsabilités

• Prepare and process IRB proposals and amendments.
• Maintain regulatory documents for sponsors and authorities.
• Participate in site visits to review research procedures.
• Identify equipment and supplies for studies.
• Screen and recruit eligible participants while ensuring compliance.
• Ensure data recorded accurately on case report forms.

Connaissances

Clinical Research

Study Design

Project Coordination

Communication

Formation

Bachelor's

Description du poste

Vanderbilt Health in the United States seeks a Clinical/Translational Research Coordinator II to coordinate approval processes and conduct of research protocols, ensuring integrity and adherence to policies.

This role involves preparing IRB submissions, maintaining regulatory documents, participating in sponsor site visits, handling data capture, and collaborating with investigators and teams across sites to keep trials on track.