Clinical Research Coordinator II

Position Summary DUTIES PERFORMED BUT NOT LIMITED TO: 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 Knowledge, Skills, and Abilities Knowledge of applicable clinical research regulatory requirements (i.e., Good Clinical Practice ( GCP ) and International Conference on Harmonization ( ICH ) guidelines) Computer skills, including proficiency in Microsoft Word, Excel, and PowerPoint Written and verbal communication skills Excellent organizational and problem-solving skills Effective time management skills and ability to manage competing priorities Minimum Qualifications Education and Experience 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 of 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, or Certified Research Administrator ( CRA ) or Clinical Research Coordinator ( CRC preferred) Preferred Qualifications #J-18808-Ljbffr Morehouse School of Medicine