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 Coordinator managing clinical trials with oversight of research data and participant compliance at Emory University. Training and guiding staff while ensuring adherence to protocols and regulations.
Responsibilities
- Independently manages significant aspects of clinical trials
- Trains and provides guidance to staff
- Oversees data management for research projects
- Interfaces with research participants and resolves study protocol issues
- Authorizes purchases for supplies and equipment maintenance
- Determines strategies for promoting/recruiting research participants
- Periodically audits operations for compliance
- Monitors IRB submissions and responds to requests
- Interfaces with study sponsors and resolves study queries
- Provides leadership in recommending and implementing improvements
- Assists in developing grant proposals and protocols
- May perform phlebotomy, specimens collection, or diagnostics
Requirements
- High School Diploma or GED with seven years of clinical research experience
- Two years of college in a scientific, health related or business administration program and five years of clinical research experience
- Licensed as a Practical Nurse (LPN) with four years of clinical research experience
- Bachelor's degree in a scientific, health related or business administration program and three years clinical research experience
- Master's degree, MD or PhD in a scientific, health related or business administration program and one year of clinical research experience
- Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred
Benefits
- Clinical research support
- In-person and potential remote work days
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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