Clinical Research Coordinator I - Hematology/Oncology

Montgomery College

Nashville (TN)

Sur place

USD 45 000 - 65 000

Plein temps

Il y a 9 jours
Générateur de candidature

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Résumé du poste

Vanderbilt Health is seeking a Clinical Translational Research Coordinator I for the Hematology/Oncology division in Nashville. You will coordinate approval processes, conduct oncology protocols, and work with investigators, IRB, and sponsors to ensure protocol integrity and regulatory compliance.

With guidance, you will screen and enroll participants, manage data, assist with budgets, and maintain communications across the study team to support study timelines and outcomes.

Qualifications

  • Bachelor's degree or equivalent experience required.
  • Phlebotomy experience preferred.
  • <1 year professional research experience required.
  • Prior coordinating hematology/oncology studies preferred.

Responsabilités

  • Coordinate approval processes and conduct oncology clinical research protocols.
  • Manage screening, recruitment, consent, enrollment, randomization, and study conduct.
  • Maintain documentation with investigators, IRB, sponsors and regulatory bodies.
  • Prepare and process IRB proposals and amendments per regulations.
  • Record data accurately in case report forms and maintain source documentation.
  • Collaborate with study teams to ensure timeline objectives are met.

Connaissances

Organizational skills
Attention to detail
Communication skills
Phlebotomy experience
Hematology/Oncology coordination

Formation

Bachelor's Degree

Outils

StarPanel

Description du poste

Vanderbilt Health is seeking a Clinical Translational Research Coordinator I for the Hematology/Oncology division in Nashville. You will coordinate approval processes, conduct oncology protocols, and work with investigators, IRB, and sponsors to ensure protocol integrity and regulatory compliance.

With guidance, you will screen and enroll participants, manage data, assist with budgets, and maintain communications across the study team to support study timelines and outcomes.

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