Georgetown University

Georgetown University

Jesuit research university in Washington, DC

Clinical Research Coordinator 1

Full-TimeDeadline 1/15/27
$47.6k - $104.7k/yr
Mid
Bachelor's
United States
In Person

On-campus work is required.

About the job

Requirements
  • A Bachelor's Degree in a scientific or health-related field is required.
  • Three to five years of related experience in clinical research is preferred.
  • Ability to work independently and function within a team.
  • Strong attention to detail.
  • Ability to prioritize competing responsibilities reliably.
  • Must comply with applicable laws and regulations, Georgetown University Medical Center policies and standard operating procedures, Human Subject Protection requirements, patient confidentiality and HIPAA, and Good Clinical Practice guidelines.
Responsibilities
  • Serve as clinical research coordinator for Phase I, II, and III oncology clinical trials conducted in the Clinical Research Management Office of Lombardi Comprehensive Cancer Center.
  • Coordinate assigned clinical trials throughout the full trial lifecycle.
  • Interface with study participants and obtain and document informed consent according to protocol, institutional policies, and regulatory guidelines for minimal-risk studies.
  • Schedule and coordinate study-related procedures and assessments while maintaining protocol integrity and patient safety in accordance with Good Clinical Practice guidelines.
  • Assist with triaging phone calls and proactive patient communication.
  • Coordinate collection of research specimens according to protocol requirements.
  • Schedule in-service training for appropriate staff on assigned clinical trials.
  • Regularly update the Clinical Trials Management System with patient information and key dates to support financial management of clinical trials.
  • Collaborate with data managers to ensure clinical trial documentation is complete and accurate, and assist with timely query resolution.
  • Schedule and facilitate sponsor meetings, including pre-study visits, site initiation visits, and monitoring visits.
  • Document and report serious adverse events according to protocol and institutional policy, with input from the principal investigator or a senior clinical research team member.
  • Act as a liaison with hospital staff, physicians, institutional review boards, review committees, the clinical research finance team, auditors, clinical research staff, and study sponsors and monitors.
  • Perform other duties as assigned.
Desired Qualifications
  • Three to five years of related experience in clinical research.

About the company

Georgetown University

Georgetown University

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Georgetown University is a private Catholic and Jesuit research university in Washington, D.C. It provides undergraduate, graduate, and professional education and conducts research across its academic community.

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