Clinical Data Coordinator for Oncology Trials

Mckesson Corporation; États-Unis; Sur place; USD 32 000 - 37 000; Plein temps

Résumé du poste

Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, seeks a Data Coordinator to support Study Coordinators in daily trials activities, ensure SOP/GCP/ICH compliance, and manage trial documentation across multiple sites. You will handle source documents, CRF completion, SAE reporting, and data-tracking tasks within the Drug Development Data Operations group.

The role requires attention to regulatory detail, strong English communication, and healthcare trial experience.

Qualifications

• Knowledge of scientific, medical, and regulatory terms.
• Knowledge of GCP and GMP.
• Detail-oriented and meticulous in documentation.
• Excellent English written and oral skills.
• Bachelor's degree preferred.
• Healthcare experience, clinical trials support, or pharmaceutical industry experience preferred.

Responsabilités

• Support Study Coordinators to meet industry trial data deadlines.
• Obtain source documentation for patients enrolled into clinical trials.
• Assist Study Coordinators with case report form completion and query resolution.
• Assist in Serious Adverse Event (SAE) reporting and tracking.
• Create and maintain patient visit tracking spreadsheets for Study Coordinators.
• Maintain and archive study administrative files.
• Participate in special procedural projects to enhance Drug Development Data Operations.
• Assess adherence to SCRI SOPs, GCP, and ICH regulations and guidelines.

Connaissances

Detail-oriented

Regulatory knowledge

English proficiency

Formation

Bachelor's degree preferred

Description du poste

Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, seeks a Data Coordinator to support Study Coordinators in daily trials activities, ensure SOP/GCP/ICH compliance, and manage trial documentation across multiple sites. You will handle source documents, CRF completion, SAE reporting, and data-tracking tasks within the Drug Development Data Operations group.

The role requires attention to regulatory detail, strong English communication, and healthcare trial experience.