Clinical Research Coordinator

Location: Onsite in Covington, Louisiana, with required travel from Covington to Kenner, Louisiana

Annual base pay: $37,800–$94,500

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Coordinate 2–6 clinical trials with varying levels of complexity.
• Recruit participants and obtain informed consent.
• Perform vital signs, phlebotomy, ECGs, and laboratory specimen processing.
• Manage regulatory documentation, study activities, and site audits.
• Collaborate with investigators, sponsors, and monitors.
• Mentor junior staff and contribute to internal training.

Requirements

• Clinical research experience at an investigative site: 1–3 years for CRC I or at least 3 years for CRC II.
• Hands-on experience with pediatric blood draws is required.
• Experience obtaining vital signs, performing phlebotomy and ECGs, and processing laboratory specimens.
• Knowledge of site operations and the drug development process.
• Strong written and verbal communication, attention to detail, and time-management skills.
• Comfort using CTMS, eCRFs, and Microsoft Office.

Culture & Benefits

• Exposure to diverse clinical trials and multiple therapeutic areas.
• Opportunities for hands-on responsibility and professional growth in clinical operations.
• Collaboration within a supportive environment that values initiative, adaptability, and continuous learning.
• Health, welfare, and other benefits may be provided depending on the position and employment schedule.