Centralized Clinical Trial Manager at ICON responsible for reviewing clinical trial site visit reports and ensuring quality standards. Act as a liaison for timely resolution of issues.
About the role
- Clinical Research Data Coordinator supporting clinical trials at Winship Cancer Institute. Coordinating and maintaining data activities related to clinical trials and collaborating with various teams.
Responsibilities
- Supports and assists in all aspects of clinical data management, protocol data management, including creation and collection of source documents, completion of case report forms, and tracking and reporting of serious adverse events
- Primary Data Coordinator (DC) for therapeutic and non-therapeutic clinical trials across all disease teams
- Reviews information from medical records to extract data for all assigned research protocols
- Accurately captures and enters data into clinical trial databases as necessary
- Collects and maintains complete records and metrics on each research study participant
- Consolidates clinical data and reports for investigators as needed
- Attends study team meetings and provides updates to study team members
Requirements
- High School Diploma or GED and three years of administrative support experience
- Two years of college in a scientific, health related, or business administration program and one year of admin support or customer service experience
- Licensed as a practical nurse (LPN) and one year admin support or one year of licensed practical nursing experience
- Bachelor's degree, Master's degree, MD or PhD in a scientific, health related or business administration program
Benefits
- Health insurance
- Professional development opportunities
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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