Clinical Trials Data Coordinator – Impact & Compliance

McKesson; Orlando, Northern (FL, KY); Hybrid; USD 55,000 - 75,000; Full time

Job summary

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, is seeking a Data Coordinator to support the Study Coordinator in daily data operations for oncology clinical trials in the United States. You will ensure SOPs, GCP, and ICH guidelines are followed while handling source documentation and data queries.

This role emphasizes attention to detail, timely data deadlines, and collaboration with cross-functional teams to maintain study files, track patient visits, and contribute to

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

• You will support the Study Coordinator to meet industry trial data deadlines
• You will obtain source documentation for patients enrolled into clinical trial
• You willassistthe Study Coordinator with case report form completion and query resolution
• You willassistin Serious Adverse Event (SAE) reporting and tracking
• You will create and maintain patient visit tracking spreadsheets for the Study Coordinator
• You will maintain and 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

Skills

GCP/GMP knowledge

Detail-oriented

Excellent English (written and oral)

Clinical trials experience

Education

Bachelor's degree preferred

Job description

Sarah Cannon Research Institute (SCRI), a McKesson subsidiary, is seeking a Data Coordinator to support the Study Coordinator in daily data operations for oncology clinical trials in the United States. You will ensure SOPs, GCP, and ICH guidelines are followed while handling source documentation and data queries.

This role emphasizes attention to detail, timely data deadlines, and collaboration with cross-functional teams to maintain study files, track patient visits, and contribute to