Clinical Research Coordinator

IQVIA•Covington, LA

40d•$37,800 - $94,500•Onsite

About The Position

This is an on site role and candidate must be able to travel from Covington LA to Kenner LA. Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. At Avacare, CRCs wear more hats than in traditional research settings. You’ll gain experience across multiple therapeutic areas, manage complex protocols, and take ownership of key trial activities — from patient recruitment and informed consent to regulatory documentation and site audits. This breadth of responsibility not only strengthens your core CRC skills but also prepares you for future roles in clinical operations, monitoring, and beyond. Whether you're early in your CRC journey or ready to take the next step, Avacare offers a unique environment where your contributions matter and your career can flourish.

Requirements

Hands-on experience in obtaining vital signs
Performing phlebotomy
Conducting ECGs
Processing lab specimens
Solid understanding of site operations and the drug development process
Experience with pediatric blood draws
Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants (for CRC I)
Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants (for CRC II)
Strong written and verbal communication skills
Attention to detail
Time management
Comfortable using CTMS, eCRFs, and Microsoft Office tools