Sponsor-Dedicated Clinical Research Associate

IQVIA; California (MO); On-site; USD 72,000 - 189,000; Full time

Job summary

IQVIA is seeking a Clinical Monitoring Associate to ensure sites conduct studies per protocol and regulatory guidelines. You will monitor visits, support subject recruitment, and maintain clear communication with site staff to manage expectations and issues.

The role requires at least 2 years of on-site monitoring experience, strong knowledge of GCP/ICH, and proficient use of MS Word, Excel, and PowerPoint. Fluent English and excellent organizational skills are essential.

Qualifications

• Bachelor's Degree in scientific discipline or health care preferred.
• Requires at least 2 years of on-site monitoring experience.
• Knowledge of GCP and ICH guidelines.
• Strong communication and organizational skills.
• Proficient with MS Word, Excel, and PowerPoint; ability to use mobile devices.

Responsibilities

• Perform site monitoring visits according to scope of work and GCP.
• Coordinate recruitment plans to meet project needs.
• Administer protocol training and maintain site communications.
• Evaluate site practices for quality and regulatory compliance; escalate issues.
• Track regulatory submissions, enrollment, CRF completion, and data queries.
• Maintain TMF and ISF documents per regulatory requirements.
• Prepare visit reports and follow-up documentation.
• Collaborate with study team for project execution.
• Support start-up and site financial management where applicable.

Skills

Site monitoring

GCP/ICH knowledge

Project coordination

English proficiency

MS Office proficiency

Education

Bachelor's Degree in scientific discipline or health care

Tools

MS Word

MS Excel

PowerPoint

Job description

IQVIA is seeking a Clinical Monitoring Associate to ensure sites conduct studies per protocol and regulatory guidelines. You will monitor visits, support subject recruitment, and maintain clear communication with site staff to manage expectations and issues.

The role requires at least 2 years of on-site monitoring experience, strong knowledge of GCP/ICH, and proficient use of MS Word, Excel, and PowerPoint. Fluent English and excellent organizational skills are essential.