Clinical Research Coordinator Ii - School Of Medicine, Surgery

Emory University

Atlanta, Georgia, United States
In-person
Manages research project databases
Interfaces with research participants
Ensures compliance with research protocols
Emory University is seeking a Clinical Research Coordinator II for its School of Medicine, specifically in the Surgery department. The role involves managing clinical trials, ensuring compliance with research protocols, and interacting with study participants, with a requirement for in-person work at Emory's location

Job Summary

  • The Clinical Research Coordinator II handles administrative activities generally associated with the conduct of clinical trials at Emory University.
  • Key responsibilities include managing research databases, determining participant eligibility, obtaining consent, and ensuring strict protocol compliance.
  • This position requires in-person work at Grady Hospital in Atlanta, GA, involving contact with human blood and potentially infectious materials.

Matching Summary

Match Score: 85

Emory University is seeking a Clinical Research Coordinator II for its School of Medicine, specifically in the Surgery department. The role involves managing clinical trials, ensuring compliance with research protocols, and interacting with study participants, with a requirement for in-person work at Emory's location.

Skills & Requirements

Must-have

  • Manages research project databases
  • Interfaces with research participants
  • Ensures compliance with research protocols
  • Performs phlebotomy or diagnostics if credentialed
  • Attends monitoring meetings with sponsors

Nice-to-have

  • Willing to work evenings and overnight shifts
  • Participate in on-call rotation as needed
  • Takes ownership of tasks and responsibilities
  • Maintains high level of productivity
  • Communicates regularly with leadership

Key Requirements

  • High School Diploma/GED plus five years experience OR Bachelor's degree plus one year experience
  • Must complete CITI/HIPAA training and Good Clinical Practice certification
  • Experience with source documents and case report forms
  • Ability to supervise specimen collection and processing
  • Credentialing for phlebotomy or diagnostics may be required

Work Rights

Not specified

Tailored Resume

Cover Letter