Clinical Trials Data Coordinator - Drive Cancer Research

Sarah Cannon Research Institute; Orlando (FL); On-site; USD 52,000 - 68,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI) is seeking a Data Coordinator to support the Study Coordinator in daily data operations for clinical trials. The role ensures SOP/GCP/ICH compliance while handling data deadlines and source documentation.

The position emphasizes attention to detail, strong English communication, and familiarity with regulatory terms. Bachelor’s degree and healthcare/clinical trials experience are preferred.

Qualifications

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

Responsibilities

• Support the Study Coordinator to meet industry trial data deadlines.
• Obtain source documentation for patients enrolled into clinical trials.
• Assist the Study Coordinator with case report form completion and query resolution.
• Assist in Serious Adverse Event (SAE) reporting and tracking.
• Create and maintain patient visit tracking spreadsheets for the Study Coordinator.
• Maintain and archive study administrative files.
• Participate in special procedural projects to enhance Drug Development Data Operations.
• Assess adherence to SCRI SOPs, GCP and ICH regulations and guidelines during the trial.

Skills

GCP GMP knowledge

Detail-oriented

English communication

Education

Bachelor's degree

Job description

Sarah Cannon Research Institute (SCRI) is seeking a Data Coordinator to support the Study Coordinator in daily data operations for clinical trials. The role ensures SOP/GCP/ICH compliance while handling data deadlines and source documentation.

The position emphasizes attention to detail, strong English communication, and familiarity with regulatory terms. Bachelor’s degree and healthcare/clinical trials experience are preferred.