
Clinical Research Coordinator III – Infectious Diseases
Emory University
full-time
Posted on:
Location Type: Hybrid
Location: Atlanta • United States
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About the role
- Independently manages significant and key aspects of a large clinical trial or all aspects of one or more small trials, or research projects.
- Trains and provides guidance to less experienced staff.
- Oversees data management for research projects.
- Interfaces with research participants and resolves issues related to study protocols.
- Authorizes purchases for supplies and equipment maintenance.
- Determines effective strategies for promoting/recruiting research participants and retaining participants in long term clinical trials.
- Periodically audits operations including laboratory procedures to ensure compliance with applicable regulations; provides leadership in identifying and implementing corrective actions/processes.
- Monitors IRB submissions and responds to requests and questions.
- Interfaces with study sponsors, monitors and reports SAEs; resolves study queries.
- Provides leadership in determining, recommending, and implementing improvements to policies/processes.
- Assists in developing grant proposals and protocols.
- With appropriate credentialing and training may perform phlebotomy, specimens collection or diagnostics.
- May perform some supervisory duties.
- Performs related approved responsibilities as required.
Requirements
- High School Diploma or GED and seven years of clinical research experience.
- Or two years of college in a scientific, health related or business administration program and five years of clinical research experience
- Or licensed as a Practical Nurse (LPN) and four years of clinical research experience
- Or bachelor's degree in a scientific, health related or business administration program and three years clinical research experience
- Or 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
- Health and Safety Information Not Applicable
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
data managementphlebotomyspecimens collectiondiagnosticsgrant proposal developmentprotocol developmentclinical trial managementauditing operationscompliance monitoringissue resolution
Soft Skills
leadershiptrainingguidancecommunicationproblem-solvingstrategic planningparticipant recruitmentparticipant retentionsupervisory skillsinterpersonal skills
Certifications
Certified Research Administrator (CRA)Clinical Research Coordinator (CRC)