Morehouse School of Medicine
Clinical Research Coordinator III
Morehouse School of Medicine, Atlanta, Georgia, United States, 30383
Overview
Morehouse School of Medicine’s ( MSM ) Institute Translational Genomic Medicine is seeking a Clinical Research Coordinator III to join our team. This position is responsible for coordinating and implementing clinical research at Morehouse School of Medicine and independently managing significant and key aspects of a large clinical trial or all aspects of one or more small trials, or research projects.
Minimum Qualifications Bachelor’s degree in a scientific, health-related or business administration program and three (3) 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.
Preferred Qualifications Seven (7) years of clinical research experience, or two (2) years of college in a scientific, health-related or business administration program and five years of clinical research experience. Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred.
Description of Job Duty DUTIES PERFORMED BUT NOT LIMITED TO: Trains and provides guidance to less experienced staff. Oversees data management for research projects.
Responsibilities
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. 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.
Seniority level Mid-Senior level
Employment type Full-time
Job function Research, Analyst, and Information Technology
Industries Higher Education
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr
Minimum Qualifications Bachelor’s degree in a scientific, health-related or business administration program and three (3) 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.
Preferred Qualifications Seven (7) years of clinical research experience, or two (2) years of college in a scientific, health-related or business administration program and five years of clinical research experience. Certified Research Administrator (CRA) or Clinical Research Coordinator (CRC) preferred.
Description of Job Duty DUTIES PERFORMED BUT NOT LIMITED TO: Trains and provides guidance to less experienced staff. Oversees data management for research projects.
Responsibilities
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. 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.
Seniority level Mid-Senior level
Employment type Full-time
Job function Research, Analyst, and Information Technology
Industries Higher Education
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr