Oncology Clinical Research Coordinator I — Entry Level

Vanderbilt Health; Nashville (TN); Sur place; USD 43 000 - 64 000; Plein temps

Résumé du poste

Vanderbilt Health is seeking a Clinical Research Coordinator to support hematology/oncology studies in the Holowatyj Laboratory & Team. The role involves coordinating approval processes, consent, enrollment, randomization, and study conduct while ensuring adherence to Good Clinical Practice, federal regulations, and sponsor guidelines.

Responsibilities include screening, recruitment, data collection, and timely communication with Investigators, IRB, sponsors, and study personnel.

Qualifications

• Bachelor's Degree (or equivalent) required.
• Phlebotomy experience preferred.
• <1 year professional research experience required.
• Prior experience coordinating hematology/oncology studies preferred.
• Exceptional organizational, attention to detail, and communication skills required.

Responsabilités

• Conveys knowledge of policies, procedures, and regulations governing human subjects research.
• Prepares and processes IRB proposals, amendments, continuing reviews, and adverse event reports.
• Coordinates with investigators, staff, and sponsors to ensure timely study conduct.
• Manages participant recruitment, screening, enrollment, and data collection.
• Maintains documentation for regulatory authorities and sponsors in compliance with GCP.

Connaissances

Phlebotomy

Research coordination

Communication

Organizational skills

Formation

Bachelor's degree or equivalent experience

Outils

StarPanel

Description du poste

Vanderbilt Health is seeking a Clinical Research Coordinator to support hematology/oncology studies in the Holowatyj Laboratory & Team. The role involves coordinating approval processes, consent, enrollment, randomization, and study conduct while ensuring adherence to Good Clinical Practice, federal regulations, and sponsor guidelines.

Responsibilities include screening, recruitment, data collection, and timely communication with Investigators, IRB, sponsors, and study personnel.