Clinical Data Coordinator – Impactful Cancer Research

MCKESSON; Denver (CO); Vor Ort; USD 32.000 - 37.000; Vollzeit

Zusammenfassung

Sarah Cannon Research Institute (SCRI) is a leading oncology research organization within McKesson that conducts community-based clinical trials across the country. The Data Coordinator supports Study Coordinators daily, ensuring SOP and GCP/ICH compliance while handling data timelines and documentation.

Role requires knowledge of medical and regulatory terminology, attention to detail, and excellent English communication.

Qualifikationen

• Knowledge of scientific, medical, and regulatory terms.
• Knowledge of GCP and GMP.
• Detail-oriented mindset with strong regulatory awareness.
• Excellent English written and oral skills.

Aufgaben

• Support Study Coordinators to meet trial data deadlines.
• Obtain source documentation for patients enrolled in trials.
• Assist in case report form completion and query resolution.
• Assist in SAE reporting and tracking.
• Create and maintain patient visit tracking spreadsheets.
• Maintain and archive study administrative files.
• Participate in special procedural projects to enhance data operations.
• Ensure adherence to SCRI SOPs, GCP and ICH guidelines throughout trials.

Kenntnisse

GCP/GMP knowledge

Detail-oriented

English proficiency

Regulatory terms knowledge

Ausbildung

Bachelor's degree preferred

Jobbeschreibung

Sarah Cannon Research Institute (SCRI) is a leading oncology research organization within McKesson that conducts community-based clinical trials across the country. The Data Coordinator supports Study Coordinators daily, ensuring SOP and GCP/ICH compliance while handling data timelines and documentation.

Role requires knowledge of medical and regulatory terminology, attention to detail, and excellent English communication.