Sarah Cannon Research Institute · 5 hours ago
Data Coordinator
Nashville, TN
Full-time
Hybrid
New Grad, Entry LevelSarah Cannon Research Institute (SCRI) is a leading oncology research organization focused on advancing cancer therapies through community-based clinical trials. The Data Coordinator will support the Study Coordinator in managing clinical trial data, ensuring compliance with regulations, and maintaining documentation.
Responsibilities
You will support the Study Coordinator to meet industry trial data deadlines
You will obtain source documentation for patients enrolled into clinical trial
You will assist the Study Coordinator 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 the Study Coordinator
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
Qualification
Required
Knowledge of scientific, medical, and regulatory terms
Knowledge of GCP and Good Manufacturing Practice (GMP)
Detail-oriented
Excellent English written and oral skills
Preferred
Bachelor Degree
Healthcare experience, Clinical trials support, or pharmaceutical industry experience
Benefits
Comprehensive benefits to support physical, mental, and financial well-being
Competitive compensation package
Annual bonus or long-term incentive opportunities
Company
Sarah Cannon Research Institute
Sarah Cannon Research Institute is one of the world’s leading oncology research organizations conducting community-based clinical trials.
Founded in 1993
501-1000 employees
Funding
Current Stage
Late StageLeadership Team
Deepak Bhamidipati
Assistant Director of Drug Development
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