About the Role

As a Clinical Research Coordinator, you will be responsible for day-to-day clinical research activities, including subject recruitment, data collection, regulatory compliance, and specimen handling. You will ensure study protocols are followed, obtain informed consent, collect and process biological specimens, perform basic clinical procedures, maintain documentation, and communicate with sponsors and regulatory bodies.

About You

Required:

Bachelor's degree in a health-related field or equivalent experience.
Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
Excellent organizational skills and attention to detail.
Strong interpersonal and communication skills.
Proficiency in Microsoft Office and electronic data capture systems.

Preferred:

At least 1–2 years of experience in clinical research.
Phlebotomy certification or Medical Assistant (MA) certification.
Experience working in clinical trials, especially in a hospital or academic setting.
Familiarity with IRB processes and clinical trial documentation.
Bilingual skills depending on patient population.

With 30+ years of experience, 28+ locations, and 2,000+ clinical studies conducted, Elite Clinical Network (ECN) is a trusted leader in clinical research. Our dedicated network of research sites is built on personalized service, investigator diversity, and rigorous quality processes to ensure excellence in every study. Backed by a professional corporate management team, we partner with top physicians across diverse specialties to accelerate clinical trials while maintaining the highest standards of compliance. Attention to detail drives everything we do—from site management to patient engagement. Whether you’re a medical professional looking to make an impact or a Sponsor/CRO seeking a trusted research partner, ECN offers unparalleled opportunities to drive medical advancements. Learn more at eliteclinicalnetwork.com

Clinical Research Coordinator

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Summary

About the Role

About You