Clinical Research Coordinator, Hematology & Oncology Trials

UCLA Health; Beverly Hills (CA); Sur place; USD 53 000 - 85 000; Plein temps

Résumé du poste

UCLA Health seeks a Clinical Research Coordinator to support the full lifecycle of clinical studies, from design through closeout.

You will implement research activities for one or more studies and organize tasks to ensure adherence to study protocols and regulatory requirements. The role involves collaboration with the Principal Investigator, ancillary departments, sponsors, and other entities to maintain compliant conduct and proper study administration.

Qualifications

• Experience coordinating clinical research trials and studies.
• Familiarity with FDA CFR and ICH-GCP guidelines.
• Ability to plan, organize, and meet study timelines.

Responsabilités

• Manage design, setup, conduct, and closeout of clinical studies.
• Implement research activities for one or more trials while meeting deadlines.
• Ensure adherence to protocols and applicable regulations and policies.
• Collaborate with PI, ancillary departments, sponsors, and sites to support study administration.

Description du poste

UCLA Health seeks a Clinical Research Coordinator to support the full lifecycle of clinical studies, from design through closeout.

You will implement research activities for one or more studies and organize tasks to ensure adherence to study protocols and regulatory requirements. The role involves collaboration with the Principal Investigator, ancillary departments, sponsors, and other entities to maintain compliant conduct and proper study administration.