Neurology Clinical Trials Coordinator – Onsite

Georgetown University; Washington (District of Columbia); On-site; USD 44,022 - 73,406; Full time

Benefits offered by this job

Medical benefits

Tuition assistance

Work-life balance benefits

Retirement savings plan

Job summary

Georgetown University seeks a Clinical Research Coordinator I to manage 7 neurology trials, coordinating visit schedules, data entry, and regulatory activities. On-site role requiring strong organization and patient interaction, with collaboration across Radiology, Pharmacy, and CROO to ensure protocol adherence and timely reporting of adverse events.

The CRCI will work five days on-site at Georgetown University Hospital and report to the Associate Director of Clinical Trials, contributing to

Qualifications

• Bachelor’s degree required with 5+ years of clinical trial coordination/assistance experience.
• Experience coordinating multiple trials, with strong organization and communication skills.
• Familiarity with regulatory requirements and adverse event reporting procedures.

Responsibilities

• Coordinate multiple clinical trials within Neurology, ensuring protocol adherence.
• Manage visit schedules, prep work, and patient visits for trial participants.
• Maintain confidentiality and coordinate with multiple departments (Radiology, CRU, Pharmacy).
• Regularly report data and adverse events to sponsors and team members.

Skills

Clinical trial coordination

Patient interaction

Regulatory knowledge

Interdepartmental communication

Education

Bachelor’s degree

5+ years clinical trial experience

Tools

OnCore/CTMS

Job description

Georgetown University seeks a Clinical Research Coordinator I to manage 7 neurology trials, coordinating visit schedules, data entry, and regulatory activities. On-site role requiring strong organization and patient interaction, with collaboration across Radiology, Pharmacy, and CROO to ensure protocol adherence and timely reporting of adverse events.

The CRCI will work five days on-site at Georgetown University Hospital and report to the Associate Director of Clinical Trials, contributing to