Cardiovascular Translational Research Coordinator II

Montgomery College; Nashville (TN); Sur place; USD 50 000 - 70 000; Plein temps

Résumé du poste

Vanderbilt Health is seeking a Clinical Research Coordinator to coordinate approval processes and conduct of clinical/translational research across sites. The role emphasizes compliance with policies, regulatory standards, and accurate data handling.

Responsibilities include IRB submissions, budgeting support, and effective communication with investigators, sponsors, and research staff. A Bachelor’s degree and clinical research experience are preferred, with opportunities within the

Qualifications

• Clinical research experience in patient-facing settings with focus on protocol follow-through.
• Familiar with informed consent, regulatory processes, IRB requirements and documentation.
• Experience collecting and managing clinical data with attention to quality and compliance.

Responsabilités

• Prepare and process IRB proposals, amendments, continuing reviews and adverse event reports.
• Maintain regulatory documents for internal and sponsor review across sites.
• Identify equipment and supplies to support study needs.
• Screen and enroll eligible participants, ensuring timely documentation.
• Record data from source documents onto case report forms with accuracy.

Connaissances

Informed consent

IRB requirements

Clinical research data

Communication

Regulatory compliance

Formation

Bachelor's degree

Outils

EDC systems

Description du poste

Vanderbilt Health is seeking a Clinical Research Coordinator to coordinate approval processes and conduct of clinical/translational research across sites. The role emphasizes compliance with policies, regulatory standards, and accurate data handling.

Responsibilities include IRB submissions, budgeting support, and effective communication with investigators, sponsors, and research staff. A Bachelor’s degree and clinical research experience are preferred, with opportunities within the