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Strong fit if you want on-site cardiology research ops at a major Atlanta academic medical center and enjoy structured, compliance-heavy coordination over remote desk work.
As a Clinical Research Coordinator II in Emory’s School of Medicine Cardiology, a typical day centers on protocol execution: screening and consenting participants, scheduling visits, collecting vitals and samples per study manuals, entering data into EDC systems, and coordinating with cardiology investigators, nurses, and sponsors. You track regulatory binders, adverse events, and visit windows so trials stay audit-ready.
No. The listing is for Atlanta, Fulton County (on-site academic/medical setting).
Emory is a private research university in Atlanta (founded 1836) with a large School of Medicine and healthcare footprint.
Free options in the provided list include Saylor Academy Health Sciences courses and Coursera audit-track healthcare courses (free to learn).
Website: emory.edu
Emory University is a private research university in Atlanta, Georgia, United States. It was founded in 1836 as Emory College by the Methodist Episcopal Church and named in honor of Methodist bishop John Emory. Its main campus is in Druid Hills, four miles from downtown Atlanta.
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Join Emory University's School of Medicine, Cardiology Department as a Clinical Research Coordinator II in Atlanta, Fulton County. This full-time position offers the opportunity to advance cardiovascular research and contribute to cutting-edge clinical trials that improve patient outcomes. About the Role The Clinical Research Coordinator II manages essential operations for clinical research studies within the Cardiology Department. You'll oversee study logistics, ensure regulatory compliance, and serve as a bridge between the research team, participants, and institutional leadership. This role is ideal for someone who thrives in a fast-paced academic medical environment and is passionate about research excellence. What You'll Do Coordinate all administrative and logistical aspects of clinical research studies from initiation through completion Recruit, screen, and enroll study participants while maintaining accurate documentation and tracking Ensure compliance with Institutional Review Board (IRB) protocols, FDA regulations, and Good Clinical Practice (GCP) standards Maintain study databases, prepare regulatory documentation, and manage informed consent processes Schedule participant visits, monitor protocol adherence, and collect clinical data with precision Communicate with principal investigators, study teams, and external stakeholders to ensure seamless study operations Prepare reports and documentation for regulatory submissions and protocol amendments What We're Looking For Bachelor's degree in life sciences, nursing, public health, or related field, or equivalent professional experience Minimum 2–3 years of clinical research coordination experience Strong knowledge of clinical trial processes, regulatory requirements, and research ethics Excellent organizational skills with ability to manage multiple studies simultaneously Proficiency with electronic data capture (EDC) systems and research databases Outstanding written and verbal communication abilities Ability to work independently while fostering collaborative relationships with research teams Commitment to accuracy, integrity, and participant safety in all research activities About Emory Emory University is a premier research institution dedicated to excellence in education, healthcare, and discovery. Our School of Medicine's Cardiology Department is renowned for innovative research that advances cardiovascular science and improves patient care. We foster an inclusive environment where talented professionals contribute to world-class research and training. How to Apply To apply, complete your application directly on this page, or you'll be redirected to the employer's application platform to finish submitting there.
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