Clinical Research Coordinator managing significant aspects of clinical trials in the School of Medicine. Overseeing data management and training less experienced staff under Emory University.
Responsibilities
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
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) and 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
Emory is an equal opportunity employer
Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status or other characteristics protected by state or federal law.
Job title
Clinical Research Coordinator III – Infectious Diseases
Research Coordinator overseeing clinical studies for musculoskeletal injuries in military health. Assisting with project planning and coordination while ensuring compliance with protocols and regulations.
Overseeing and administering clinical research studies and managing study budgets for military health research. Coordinating project planning and ensuring compliance with regulatory requirements.
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.
Clinical Research Nurse Coordinator managing clinical research operations at Duke's Trauma, Acute & Critical Care Division. Supervising nursing care and ensuring accuracy in data management.
Clinical Research Coordinator managing clinical trials at Emory University. Overseeing research projects, providing guidance, and ensuring compliance with protocols and regulations.
Senior Clinical Trial Manager managing Phase 1 clinical research studies and collaborating with cross - functional teams in a global biopharmaceutical environment.
HR Manager for Clinical Research Units lead engagement strategies at Fortrea. Partnering closely with site leadership in clinical environments in Dallas, TX or Madison, WI.
Clinical Trial Manager overseeing clinical trials managing operations and compliance in Brazil at IQVIA. Ensuring adherence to protocols and managing country - specific requirements.
Feasibility Manager evaluating clinical trial sites to advance pipeline and create strategic partnerships. Play a pivotal role in bringing clinical trials to life in Argentina.