Aerotek

Clinical Research Coordinator

New York, New York, United States
Full-time
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Posted 2 weeks ago

Job Description

ABOUT COMPANY:

One of the nation's leading urban medical centers.

QUALIFICATIONS:
2+ years clinical research coordinator
2+ years regulatory IRB submission
Must have patient interaction from enrolling, screening patients

JOB DUTIES:
Working for a Principal Investigator on a clinical trial, the Clinical Research Coordinator is responsible for:
* Ensuring study is compliant with local and federal laws and regulations;
* Advertising, recruitment and follow-up, including screening potential study participants;
* Preparation and submission of IRB application for approval, along with Principal Investigator and/or study staff;
* Performing initial intake assessments;
* Coordinating and scheduling follow-up visits with the appropriate location and personnel, including the CTSC;
* Creating and/or maintaining all documents and study records related to the study;
* Answer and address study participants questions and concerns;




About Aerotek:

Your success starts with the right career opportunity. Aerotek uses a people-focused approach to connect job seekers to incredible opportunities with leading organizations. Established in 1983, we've grown to become a consistent Best of Staffing® winner for talent satisfaction because of our dedication to exceptional service. Serving over 300,000 contract workers every year, we specialize in placing workers with engineering, scientific, professional and industrial skill sets. Aerotek is proud to offer competitive benefits, including contributory medical, dental and vision insurance, weekly pay, discounts on consumer goods and services and more.

Job Details

Date Posted
Nov 07, 2025
Application Deadline
Nov 15, 2035

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