Clinical Research Monitor & Site Liaison

IQVIA Inc; Durham (NC); On-site; USD 75,000 - 175,000; Full time

Job summary

IQVIA Inc. is seeking a Clinical Monitoring professional to ensure sites conduct studies per protocol, GCP, and ICH guidelines. You will monitor visits, support site training, and manage regulatory submissions and data related tasks.

The role involves coordinating with study teams, tracking enrollment, and maintaining documentation in TMF/ISF as required by local regulations. Strong English communication and organizational skills are essential.

Qualifications

• Bachelor's degree in a scientific discipline or health care preferred.
• Equivalent combination of education, training and experience may be accepted in lieu of degree.
• Some organizations require CRA training or prior monitoring experience.
• Basic knowledge of GCP and ICH guidelines.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) following scope and regulatory requirements.
• Collaborate with sites to drive and track subject recruitment plans.
• Administer protocol training and maintain regular communication with sites.
• Evaluate site practices for protocol conduct and regulatory compliance; escalate issues.

Skills

English proficiency

Communication

Organization

Microsoft Word

Excel

PowerPoint

Financial management

Education

Bachelor's Degree

Tools

Microsoft Word

Excel

PowerPoint

Job description

IQVIA Inc. is seeking a Clinical Monitoring professional to ensure sites conduct studies per protocol, GCP, and ICH guidelines. You will monitor visits, support site training, and manage regulatory submissions and data related tasks.

The role involves coordinating with study teams, tracking enrollment, and maintaining documentation in TMF/ISF as required by local regulations. Strong English communication and organizational skills are essential.