Join a dedicated clinical research team in Manhattan as a Clinical Research Specialist, responsible for launching and managing a new clinical study. This role involves end-to-end coordination of trial activities, ensuring adherence to protocols, timelines, and regulatory standards.
Key Responsibilities
- Lead the planning and execution of a new clinical trial, ensuring all phases run efficiently and in compliance
- Support the Principal Investigator in identifying and enrolling eligible patients
- Coordinate communication between sponsors, monitors, department staff, and institutional review boards
- Oversee administrative processes related to compliance, budgeting, staffing, and documentation
- Ensure accurate data collection and maintain records using electronic data capture (EDC) systems
Qualifications
Candidates should have 1–2 years of experience as a study coordinator in a hospital or outpatient setting. Strong organizational skills, attention to detail, and the ability to collaborate effectively are essential. Proficiency in MS Office, Outlook, and Internet Explorer is required.
Experience with imaging-based trials and EDC platforms is preferred. The ideal candidate is a flexible, solutions-oriented professional who maintains a high standard of ethics and accuracy in all aspects of clinical research.
Work Environment
This is a full-time, on-site position based in Manhattan, operating Monday through Friday. The role requires close collaboration with multidisciplinary teams in a fast-paced clinical setting.
