Cardiovascular Translational Research Coordinator II

Vanderbilt Health; Nashville (TN); Híbrido; USD 55.000 - 90.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Comprehensive benefits package

Health, disability, retirement and/or

Descripción de la vacante

Vanderbilt Health is seeking a Clinical Research Coordinator to coordinate IRB submissions, regulatory compliance, and patient enrollment across multiple trials. You will ensure data quality and timely documentation, collaborating with investigators, study staff, and sponsors.

Responsibilities include preparing regulatory documents, managing budgets, and ensuring adherence to GCP and regulatory standards while supporting patient safety and study integrity.

Formación

• Clinical research experience in patient-facing settings.
• Experience obtaining informed consent and educating patients.
• Familiarity with regulatory requirements and IRB.
• Experience with patient screening and eligibility assessments.
• Knowledge of regulatory documentation and trial processes.
• Experience collecting and maintaining clinical research data.
• Proficiency with electronic data capture systems.
• Strong attention to detail and regulatory compliance.
• Excellent communication and collaboration skills.

Responsabilidades

• Prepares and processes IRB proposals and amendments per policies and regulations.
• Maintains documents and participates in site visits for regulatory review.
• Identifies equipment and supplies for project needs across sites.
• Determines study participant eligibility and manages recruitment strategies.
• Records data onto case report forms with accuracy and timeliness.
• Performs specimen shipping per guidelines and maintains documentation.
• Develops and manages study budgets and billing compliance.
• Acts as advocate for human subjects with investigators and sponsors.
• Participates in ongoing informed consent process and staff councils.

Conocimientos

Clinical research

Informed consent

IRB/regulatory

Screening/eligibility

Data management

Electronic data capture

Communication/collaboration

Educación

Bachelor's degree

Herramientas

EDC systems

Descripción del empleo

Vanderbilt Health is seeking a Clinical Research Coordinator to coordinate IRB submissions, regulatory compliance, and patient enrollment across multiple trials. You will ensure data quality and timely documentation, collaborating with investigators, study staff, and sponsors.

Responsibilities include preparing regulatory documents, managing budgets, and ensuring adherence to GCP and regulatory standards while supporting patient safety and study integrity.