Clinical Research Coordinator (29674)
$70,000–$70,000 year
On-site · The Bronx, New York, United States
Job Summary
The Clinical Research Coordinator (CRC) is responsible for executing clinical trials while ensuring high standards of patient care. Key responsibilities include performing ECGs and phlebotomy related tasks, monitoring patients for Adverse Events, directing participant screening and enrollment, conducting Informed Consent processes, and coordinating patient visits and tests. The role requires a Bachelor’s degree in Science and a minimum of two years of related experience, along with strong phlebotomy skills and a solid understanding of clinical research guidelines and regulations.
Required Qualifications
- Bachelor’s Degree in Science
- Minimum of Two (2) years’ research coordinator experience
- Excellent phlebotomy skills
- Strong understanding of clinical trial phases, FDA regulations, and ICH-GCP guidelines
- Exceptional attention to detail and strong organizational skills
- Proficiency with Electronic Medical Records (EMR) and Electronic Data Capture (EDC) systems
Desired Qualifications
- Certification as a Clinical Research Professional (CCRP via SOCRA)
- Certification as a Clinical Research Coordinator (CCRC via ACRP)
- Current Good Clinical Practice (GCP) and Human Subject Protection (HSP) training
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