Neurology Clinical Research Coordinator (On-Campus)

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

Job summary

Georgetown University Hospital in Washington, DC seeks a Clinical Research Coordinator 2 to manage seven Neurology trials within the department, coordinating visits, ensuring protocol compliance, and maintaining trial data. You will interact with Radiology, CRU, and sponsors while safeguarding patient confidentiality and adhering to university research standards.

The role requires multi-year experience in clinical trials, strong organizational skills, and the ability to respond to patient

Qualifications

• Bachelor's degree, at minimum or Associate's Degree and 5 years' minimum work experience as a Clinical Trial Coordinator or Clinical Research Assistant.
• + 5 year CTC experience
• 3 years of experience working in a clinical setting that involves direct patient interaction, in a full time, part
• time, or extensive volunteer experience.
• 2 year min. experience will be as a ClinicalTrial Coordinator, Clinical Research Assistant, or equivalent position.

Responsibilities

• Manage and coordinate 7 of approximately 55 ongoing clinical trials in Neurology.
• Maintain regulatory documentation and ongoing training requirements.
• Accurate reporting of visits via OnCore/CTMS and timely data entry.
• Timely communication with team members and clinical trial sponsors.
• Coordinate interactions with Ancillary departments (Radiology, CRU, Cardiology) for visits.

Skills

Patient interaction

Regulatory compliance

Study coordination

Communication with sponsors

Data entry

Education

Bachelor's degree, at minimum

Associate's Degree

Tools

OnCore/CTMS

Radiology coordination

Job description

Georgetown University Hospital in Washington, DC seeks a Clinical Research Coordinator 2 to manage seven Neurology trials within the department, coordinating visits, ensuring protocol compliance, and maintaining trial data. You will interact with Radiology, CRU, and sponsors while safeguarding patient confidentiality and adhering to university research standards.

The role requires multi-year experience in clinical trials, strong organizational skills, and the ability to respond to patient