Clinical Research Coordinator: Multitrial Ops & Growth

IQVIA LLC; Covington (LA); Hybrid; USD 38.000 - 95.000; Vollzeit

Zusammenfassung

IQVIA is seeking a Clinical Research Coordinator for an on-site role in Covington, LA, with travel to Kenner, LA. You will support patient recruitment, informed consent, regulatory documentation, and site audits across diverse trials.

You will gain exposure to multiple therapeutic areas, manage trial activities end-to-end, and collaborate with investigators, sponsors, monitors, and junior staff in a fast-paced SMO/CRO environment.

Qualifikationen

• Hands-on experience in obtaining vital signs, performing phlebotomy, conducting ECGs, and processing lab specimens.
• Solid understanding of site operations and the drug development process. Must have experience with pediatric blood draws.
• CRC I: Minimum of 1-3 years in clinical research setting at a clinical investigative site working with participants.
• CRC II: Minimum of 3 years as a Clinical Research Coordinator in a clinical investigative site working with participants.
• Strong written and verbal communication skills, with attention to detail and time management.
• Comfortable using CTMS, eCRFs, and Microsoft Office tools.

Aufgaben

• Manage 2-6 trials of varying complexity, perform clinical procedures, and lead study coordination from start to finish.
• Coordinate patient recruitment and informed consent processes.
• Prepare and maintain regulatory documentation and conduct site audits.
• Collaborate with investigators, sponsors, and monitors; mentor junior staff.
• Work across multiple therapeutic areas and support site operations.
• Use CTMS and eCRFs in daily work.

Kenntnisse

Vital signs

Phlebotomy

ECGs

Lab specimen handling

Tools

CTMS

eCRFs

Microsoft Office

Jobbeschreibung

IQVIA is seeking a Clinical Research Coordinator for an on-site role in Covington, LA, with travel to Kenner, LA. You will support patient recruitment, informed consent, regulatory documentation, and site audits across diverse trials.

You will gain exposure to multiple therapeutic areas, manage trial activities end-to-end, and collaborate with investigators, sponsors, monitors, and junior staff in a fast-paced SMO/CRO environment.