Clinical Trials Data Coordinator

McKesson; Denver (CO); On-site; USD 32,000 - 37,000; Full time

Benefits offered by this job

Total Rewards package

Annual bonus opportunities

Job summary

Sarah Cannon Research Institute (SCRI) is seeking a Data Coordinator to support Study Coordinators in daily activities, ensuring adherence to SOPs, GCP and ICH. You will help manage source documents, CRF completion, SAE reporting, and data tracking across trials.

The role requires detail orientation, knowledge of regulatory terms, and strong English communication. Bachelor’s degree preferred; healthcare or clinical trials experience is a plus.

Qualifications

• Knowledge of scientific, medical and regulatory terms.
• Solid understanding of GCP and GMP guidelines.
• Excellent written and oral English skills.

Responsibilities

• Support Study Coordinators to meet trial data deadlines.
• Obtain source documentation for patients enrolled in trials.
• Assist with case report form completion and query resolution.
• Assist in Serious Adverse Event reporting and tracking.
• Maintain patient visit tracking spreadsheets and study files.
• Support special procedural projects to improve data operations.

Skills

GCP knowledge

GMP knowledge

Detail-oriented

English communication

Education

Bachelor's degree preferred

Job description

Sarah Cannon Research Institute (SCRI) is seeking a Data Coordinator to support Study Coordinators in daily activities, ensuring adherence to SOPs, GCP and ICH. You will help manage source documents, CRF completion, SAE reporting, and data tracking across trials.

The role requires detail orientation, knowledge of regulatory terms, and strong English communication. Bachelor’s degree preferred; healthcare or clinical trials experience is a plus.