Neuro Trials: Clinical Research Coordinator I

Montefiore Hudson Valley Collaborative; New York (NY); Hybrid; USD 46,000 - 57,000; Full time

Job summary

Montefiore Hudson Valley Collaborative is seeking a Clinical Research Coordinator I in the Bronx, NY, to oversee multiple neurologic clinical trials, investigator-initiated studies, and quality improvement projects. You will coordinate with departments hospital-wide, ensure protocol adherence, and support patient and family communication.

The role requires a BS, GCP/IRB compliance knowledge, and strong organizational skills to manage data, regulatory documents, and trial logistics.

Qualifications

• BS in a related field required.
• Experience in clinical research or trials.
• Certification in GCP and related topics.

Responsibilities

• Direct daily trial-related activities, recruitment and assessments of participants.
• Ensure adherence to study protocols and regulatory requirements.
• Design workflows for clinical trials and coordinate cross-departmental teams.
• Execute IRB submissions and regulatory reporting.
• Maintain regulatory binders and assist audits/monitors.

Skills

Clinical research experience

Regulatory knowledge

Team coordination

Education

Bachelor’s degree in a related field

CITI Good Clinical Practice Certification

CITI Research with Biomedical Drugs andDevices Certification

CITI Dangerous Goods and Biospecimen Handling Certification

Tools

EDC systems

Imaging portals

Job description

Montefiore Hudson Valley Collaborative is seeking a Clinical Research Coordinator I in the Bronx, NY, to oversee multiple neurologic clinical trials, investigator-initiated studies, and quality improvement projects. You will coordinate with departments hospital-wide, ensure protocol adherence, and support patient and family communication.

The role requires a BS, GCP/IRB compliance knowledge, and strong organizational skills to manage data, regulatory documents, and trial logistics.