Clinical Data Coordinator — Oncology Trials Support

Sarah Cannon Research Institute; Orlando (FL); On-site; USD 52,000 - 76,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI) is a leading oncology research organization enabling community-based clinical trials across the United States. The Data Coordinator role supports the Study Coordinator to meet trial data deadlines, collect source documentation, complete case report forms, and track SAE reporting and visit logs.

SCRI emphasizes regulatory compliance (GCP/ICH) and SOP adherence while offering opportunities to contribute to drug development data operations and broader cancer

Qualifications

• Knowledge of scientific, medical, and regulatory terms.
• Knowledge of GCP and GMP.
• Detail-oriented.
• Excellent English written and oral skills.
• Bachelor Degree preferred.
• Healthcare experience, Clinical trials support, or pharmaceutical industry experience preferred.

Responsibilities

• You will support the Study Coordinator to meet industry trial data deadlines.
• You will obtain source documentation for patients enrolled into clinical trial.
• You will assistthe Study Coordinator with case report form completion and query resolution.
• You willassistin Serious Adverse Event (SAE) reporting and tracking.
• You will create andmaintainpatient visit tracking spreadsheets for the Study Coordinator.
• You willmaintainand archive study administrative files.
• You will be assigned special procedural projects to enhance the functioning of Drug Development Data Operations.
• Throughout the conduct of the clinicaltrialyou will assess adherence to SCRI SOPS, Good Clinical Practice (GCP) and ICH regulations and guidelines.

Education

Bachelor degree

Job description

Sarah Cannon Research Institute (SCRI) is a leading oncology research organization enabling community-based clinical trials across the United States. The Data Coordinator role supports the Study Coordinator to meet trial data deadlines, collect source documentation, complete case report forms, and track SAE reporting and visit logs.

SCRI emphasizes regulatory compliance (GCP/ICH) and SOP adherence while offering opportunities to contribute to drug development data operations and broader cancer