Sarah Cannon Research Institute · 2 days ago

Data Coordinator

Nashville, TN

Full-time

Hybrid

Entry Level

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Responsibilities

Support Study Coordinator to meet industry trial data deadlines

Obtain source documentation for patients enrolled in clinical trials

Assist Study Coordinator with case report form completion and query resolution

Assist in Serious Adverse Event (SAE) reporting and tracking

Create and maintain patient visit tracking spreadsheets

Maintain and archive study administrative files

Work on special procedural projects to enhance Drug Development Data Operations

Assess adherence to SCRI SOPs, GCP, and ICH regulations throughout the clinical trial conduct

Qualification

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scientific terms medical terms regulatory terms GCP Good Manufacturing Practice (GMP)Detail-oriented communication skillsHealthcare experienceClinical trials supportPharmaceutical industry experience