Clinical Data Coordinator — Trials Support & SAE Tracking

Sarah Cannon Research Institute; Denver (CO); Vor Ort; USD 32.000 - 37.000; Vollzeit

Zusammenfassung

Sarah Cannon Research Institute (SCRI) is seeking a Data Coordinator to support Study Coordinators in daily trial operations and ensure all activities comply with SOPs, GCP, and ICH guidelines. The role emphasizes data deadlines, source documentation, and SAE tracking in a leading oncology clinical trial network.

You will contribute to data integrity and operational efficiency across Drug Development Data Operations, with opportunities to engage in special projects and professional development

Qualifikationen

• Knowledge of GCP and GMP.
• Detail-oriented.
• Excellent English written and oral skills.
• Bachelor’s degree preferred.
• Healthcare experience, clinical trials support, or pharmaceutical industry experience preferred.

Aufgaben

• You will support Study Coordinators to meet industry trial data deadlines
• You will obtain source documentation for patients enrolled into clinical trial
• You will assist Study Coordinators with case report form completion and query resolution
• You will assist in Serious Adverse Event (SAE) reporting and tracking
• You will create and maintain patient visit tracking spreadsheets for Study Coordinators
• 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 clinical trial, you will assess adherence to SCRI SOPs, Good Clinical Practice (GCP) and ICH regulations and guidelines.

Kenntnisse

Detail-oriented

Excellent English

GCP/GMP knowledge

Ausbildung

Bachelor’s degree preferred

Jobbeschreibung

Sarah Cannon Research Institute (SCRI) is seeking a Data Coordinator to support Study Coordinators in daily trial operations and ensure all activities comply with SOPs, GCP, and ICH guidelines. The role emphasizes data deadlines, source documentation, and SAE tracking in a leading oncology clinical trial network.

You will contribute to data integrity and operational efficiency across Drug Development Data Operations, with opportunities to engage in special projects and professional development