Senior Clinical Research Coordinator – Trial Leadership

Emory University

Atlanta (GA)

On-site

USD 70,000 - 110,000

Full time

3 days ago
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Job summary

Emory University in Atlanta seeks an experienced clinical research professional to manage major aspects of trials, oversee data management, and train staff. This role is primarily in-person at an Emory location, with possible remote work days subject to department discretion.

The position requires strong regulatory knowledge, ability to coordinate with sponsors and IRBs, and may include phlebotomy responsibilities. A relevant degree and hands-on clinical research experience are expected.

Qualifications

  • Clinical research experience required, with relevant credentialing considered.
  • Advanced degrees or CRA/CRC certification preferred.
  • Experience coordinating multi-site clinical trials and data management.

Responsibilities

  • Manage significant aspects of clinical trials or multiple small trials.
  • Train and guide less experienced staff.
  • Oversee data management for research projects.
  • Interface with participants and resolve protocol issues.
  • Authorize purchases for supplies and equipment maintenance.
  • Promote/recruit research participants and retain them long-term.
  • Audit operations for regulatory compliance and drive corrective actions.
  • Monitor IRB submissions and respond to requests.
  • Interface with sponsors, monitors and report SAEs.
  • Contribute to policy/process improvements.
  • Assist in developing grant proposals and protocols.
  • May perform phlebotomy or specimen collection with credentialing.
  • May perform supervisory duties.
  • Perform related approved responsibilities.

Job description

Emory University in Atlanta seeks an experienced clinical research professional to manage major aspects of trials, oversee data management, and train staff. This role is primarily in-person at an Emory location, with possible remote work days subject to department discretion.

The position requires strong regulatory knowledge, ability to coordinate with sponsors and IRBs, and may include phlebotomy responsibilities. A relevant degree and hands-on clinical research experience are expected.

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