Title: Clinical Data Coordinator
Location: Brentwood, TN (ONSITE ROLE)
Type: 6 month Contract
Schedule: Core business hours M-F
Start Date: ASAP
Responsibilities:
- Support data entry activities to meet study data needs and deadlines
- Data abstraction from diverse sources
- Obtain source documentation for patients enrolled into clinical trials and data registry
- Maintain Data Registry as directed
- Supports Clinical Project Manager to meet industry trial data deadlines
- Obtain source documentation for patients enrolled into clinical trial
- Assist in SAE reporting and tracking
- Create and maintain patient visit tracking spreadsheets
- Maintain and archive study documents
- Attend meetings as assigned and report on actions
- All other duties as assigned
Requirements:
- High School Diploma Required
- Bachelor’s Degree Preferred
- 1+ years of experience in healthcare, research, or other science related field
- Knowledge of scientific, medical, and regulatory terms
- Must have an understanding of clinical research process
- Knowledge of GCP and GMP
- Computer skills with ability to use clinical trial databases, electronic data capture, MS Access or Excel
Ref: #568-Clinical
