Data Coordinator

The Data Coordinator provides support to Study Coordinator on a daily basis, ensures all activities are conducted according to company standard operating procedures (SOPs) and all applicable Good Clinical Practice (GCP) and ICH regulations and guidelines.

• Provides support to Study Coordinator on a daily basis
• Ensures all activities are conducted according to company standard operating procedures (SOPs) and all applicable Good Clinical Practice (GCP) and ICH regulations and guidelines
• Supports the Study Coordinator to meet industry trial data deadlines
• Obtains source documentation for patients enrolled into clinical trial
• Assists the Study Coordinator with case report form completion and query resolution
• Assists in Serious Adverse Event (SAE) reporting and tracking
• Creates and maintains patient visit tracking spreadsheets for the Study Coordinator
• Maintains and archives study administrative files
• Assists in special procedural projects to enhance the functioning of Drug Development Data Operations

• Knowledge of scientific, medical, and regulatory terms
• Knowledge of GCP and Good Manufacturing Practice (GMP)
• Detail-oriented
• Excellent English written and oral skills

• 401k matching
• Health insurance
• Flight privileges

Sarah Cannon Research Institute (SCRI) is one of the world’s leading oncology research organizations conducting community-based clinical trials.