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Morehouse School Of Medicine

Clinical Research Coordinator III

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What they do

A Clinical Research Coordinator directs clinical research and development projects for companies, and coordinates testing and quality control.

$111,453 / year median in Georgia

+15% projected growth

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Job Description

Clinical Research Coordinator III Morehouse School Of Medicine - 3.4 Atlanta, GA Job Details 10 hours ago Qualifications Quality control corrective actions Managing scientific research projects Doctor of Medicine Master's degree in business administration Staff supervision Laboratory procedures CCRC Microsoft Excel Management Assisting with diagnostic tests and procedures Phlebotomy specimen handling Bachelor's degree in business administration High school diploma or GED Research industry grant writing Medical diagnostic testing ICH guidelines Clinical staff training Policy & process development Bachelor's degree Laboratory regulatory affairs Data management Doctor of Philosophy Scientific protocols Staff training Managing clinical research teams Mentoring Purchasing Implementing research protocols Communication with regulatory authorities for clinical trials LPN Full Job Description Please see Special Instructions for more details. Employment in this role may be contingent upon extramural funding and successful performance and may be terminated or reduced in percentage of appointment if such funding is not secured or ceases to be available. The Clinical Research Coordinator III reports to the Assistant Director, Clinical Trials and Principal Investigator(s).

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 Closing Date 12/09/2026 Open Until Filled No Special Instructions to Applicants Employment in this role may be contingent upon extramural funding and successful performance and may be terminated or reduced in percentage of appointment if such funding is not secured or ceases to be available.

Quick Link https:

//careers.msm.edu/postings/24532 EEO Statement Summary Morehouse School of Medicine is an equal opportunity/equal access/affirmative action employer fully committed to achieving a diverse workforce and complies with all Federal and Georgia State laws, regulations, and executive orders regarding non-discrimination and affirmative action. Morehouse School of Medicine does not discriminate on the basis of race, age, color, religion, national origin or ancestry, sex, gender, disability, veteran status, genetic information, sexual orientation, or gender identity or expression. Job Duties Pre-Employment/Employment Requirements All offers of employment are contingent upon successful completion of all pre-employment screenings. Immunization Immunization Requirements It is MSM's Immunization policy that all Prospective Employees are encouraged to provide proof that they are vaccinated against

COVID-19

prior to commencement of employment. If employment will commence during Flu Season, MSM requires all individuals to provide proof that they are vaccinated against Seasonal Influenza for the current Flu Season, unless granted an exemption. Failure to provide proof of vaccination for any required vaccines or obtain an exemption from MSM will result in rescission of a candidate's offer of employment or disciplinary action up to and including termination. Posting Specific Questions Required fields are indicated with an asterisk (

•). Applicant Documents Required Documents Curriculum Vitae or Resume Optional Documents Cover Letter

Benefits

  • Dental Insurance