Study Research Coordinator| Diagnostic & Treatment Center (2 positions available)

Rockefeller University • New York, NY

51d • $110,000 - $125,000 • Onsite

About The Position

The new Diagnostic and Treatment Center (D&TC) will be named the “Rockefeller University Clinical Research Center” (RCRC). The University remains committed to its mission of improving the understanding of science for the benefit of humanity through both clinical and basic research in a diverse range of biological and biomedical issues. The outpatient D&TC reflects the evolution in clinical research to outpatient studies.
Overview

Two (2) positions available
Reporting to the Clinical Research Coordinator (NP), the Study Research Coordinator focuses on trial operations and participants, coordinating day-to-day activities and assisting investigators with preparing IRB applications and submitting them to the Diagnostic and Treatment Center (D&TC).

Requirements

• A bachelor’s degree in a related field is required.
• Must possess a minimum of 3 years of clinical research experience.
• Position requires in-person, onsite presence.
• Organization, discretion, judgment, and analytical ability.
• Must be proficient in computer platforms, including MS Office Suite. Strong technical proficiency and quantitative skills are required. Must have the highest level of discretion to handle confidential information.
• Effective communication with patients, families, physicians, and staff. Strong teamwork and leadership skills at the study level. Ability to adapt to multiple priorities.
• Must have a passion for excellent customer service and commitment to exceptional quality. Strong interpersonal, written, and oral communication skills, along with attention to detail, are essential. Initiative and self-motivation are critical.

Nice To Haves

• Prior clinical trial experience preferred.
• Preferred: CCRC (ACRP) or CCRP (SOCRA).
• Prior experience in an academic or research institution is strongly preferred.

Responsibilities

• Assists investigators with building IRB applications and submissions; Performs an audit of studies they are not directly coordinating.
• Screens, enrolls, and monitors participants, ensuring accurate data collection, documentation, and organization.
• Safeguards participant safety.
• Communicates with study teams, patients, and physicians. Manages workflow independently with the highest level of attention to detail.
• Audits ongoing protocols and performs other duties and special projects as assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level