Senior Clinical Trial Manager at ICON managing clinical trial responsibilities and fostering stakeholder relationships. Overseeing budgets, study oversight, and driving enrollment in trials.
About the role
- Clinical Research Data Coordinator supporting clinical data management and protocol data management at Emory University. Involves data extraction, consolidation, and compliance with research protocols.
Responsibilities
- Supports and assists in all aspects of clinical data management and protocol data management
- Reviews information from medical records to extract data for all assigned research protocols
- Consolidates clinical data and reports for investigators as needed
- Prepares for and assists with internal quality control audits
- Provides support during internal and external monitoring and auditing
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
- Emory is an equal opportunity employer
- Participation in university programs
- Reasonable accommodations for individuals with disabilities
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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