Onsite Neurology Clinical Trials Coordinator

Georgetown University

Center (IN)

On-site

INR 4,209,000 - 7,018,000

Full time

4 days ago
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Benefits offered by this job

Medical, dental, vision insurance
Disability and life insurance
Retirement savings
Tuition assistance
Work-life balance benefits

Job summary

Georgetown University Hospital in Washington, DC seeks a Clinical Research Coordinator I for Neurology trials. You will coordinate seven studies, manage patient visits, and ensure protocol adherence within a busy clinical research environment on-site.

The CRCI will work closely with the Associate Director of Clinical Trials, CROO, CRU, and sponsors to maintain study timelines and data integrity. Applicants should have a Bachelor's degree and at least five years of clinical trial coordination

Qualifications

  • Bachelor’s degree required with clinical trial experience.
  • Minimum 5 years’ experience as Clinical Trial Coordinator or equivalent.
  • Experience with neurology trials and patient care preferred.
  • Ability to read and interpret patient medical records and trial protocols.
  • Familiarity with regulatory requirements and data reporting.

Responsibilities

  • Coordinate 7 studies within a portfolio of ~55 ongoing trials.
  • Manage patient visits, scheduling, and protocol adherence.
  • Maintain regulatory compliance and timely reporting of events.
  • Enter data accurately in CTMS/oncore systems and communicate with sponsors.

Skills

Clinical Trial Coordination
Regulatory compliance
Patient interaction
Multi-study coordination
Data entry / reporting

Education

Bachelor's degree

Tools

OnCore/CTMS
EMR/EHR systems

Job description

Georgetown University Hospital in Washington, DC seeks a Clinical Research Coordinator I for Neurology trials. You will coordinate seven studies, manage patient visits, and ensure protocol adherence within a busy clinical research environment on-site.

The CRCI will work closely with the Associate Director of Clinical Trials, CROO, CRU, and sponsors to maintain study timelines and data integrity. Applicants should have a Bachelor's degree and at least five years of clinical trial coordination

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