georgetown

Clinical Research Coordinator 1

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At a Glance

Location
Medical Center, United States
Employment
Full time
Compensation
The projected salary $20.16 - $31.30 Compensation is determined by
Posted
2026-07-28

Key Requirements

Required Skills

GCP

Domain Knowledge

  • Clinical
  • Education
  • Finance
  • Medical
  • Regulatory

Requirements

Serves as clinical research coordinator for phase I, II, and III oncology clinical trials conducted in the Lombardi Comprehensive Cancer Center.

Adheres to Georgetown University Medical Center’s philosophies, policies, and SOPs.

Works in compliance with Human Subject Protection regulations, patient confidentiality/HIPAA requirements, and Good Clinical Practice.

Responsible for overall coordination of assigned clinical trials throughout the trial lifecycle.

Collaborate with investigators and more senior study team members by participating in recruitment and selection of study participants; document and collect data to support protocol screening and determine compliance with eligibility requirements.

Interface with study participants and obtain and document informed consent according to protocol, institutional policies, and regulatory guidelines.

Compensation & Benefits

The

projected salary

$20.16 - $31.30

Compensation is determined by a number of factors including, but not limited to, the candidate’s individual qualifications, experience, education, skills, and certifications, as well as the University’s business needs and external factors.

Current Georgetown Employees:

Responsibilities

Serves as clinical research coordinator for phase I, II, and III oncology clinical trials conducted in the Lombardi Comprehensive Cancer Center.

Adheres to Georgetown University Medical Center’s philosophies, policies, and SOPs.

Works in compliance with Human Subject Protection regulations, patient confidentiality/HIPAA requirements, and Good Clinical Practice.

Responsible for overall coordination of assigned clinical trials throughout the trial lifecycle.

Collaborate with investigators and more senior study team members by participating in recruitment and selection of study participants; document and collect data to support protocol screening and determine compliance with eligibility requirements.

Interface with study participants and obtain and document informed consent according to protocol, institutional policies, and regulatory guidelines.

About the Company

, as well as

. You also can also contact the Office for Equal Opportunity Compliance at (202) 687-4798 or

oeoc@georgetown.edu

.

Need some assistance with the application process? Please call 202-687-2500. For more information about the suite of benefits, professional development and community involvement opportunities that make up Georgetown's commitment to its employees, please visit the Georgetown Works