Clinical Research Associate - Sponsor Dedicated

Location: Overland Park, Kansas, United States

Salary: $90,200–$190,000 annual base pay

Company

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

What you will do

• Conduct site selection, initiation, monitoring, and close-out visits in accordance with Good Clinical Practice and the contracted scope of work.
• Support subject recruitment plans and track recruitment, enrollment, regulatory submissions, approvals, and study progress.
• Train assigned sites on study protocols and maintain regular communication to manage expectations and resolve issues.
• Evaluate site practices, escalate quality issues, and ensure compliance with protocols and applicable regulations.
• Maintain Trial Master File and Investigator's Site File documentation, visit reports, follow-up letters, and action plans.
• Collaborate with study teams and, where applicable, support site financial management and invoice retrieval.

Requirements

• Bachelor's degree in a scientific or healthcare discipline preferred; equivalent education, training, and experience may be accepted.
• At least 1.5 years of on-site monitoring experience.
• Knowledge of clinical research regulations, Good Clinical Practice, and International Conference on Harmonization guidelines.
• Therapeutic and protocol knowledge, strong organizational and problem-solving skills, and effective time and financial management.
• Proficiency with Microsoft Word, Excel, PowerPoint, laptops, and applicable mobile devices.
• Good command of English and effective written and verbal communication skills.

Culture & Benefits

• Full-time employment with potential incentive plans, bonuses, and health and welfare benefits.
• Work focused on advancing medical treatments, improving patient outcomes, and supporting population health.
• Equal opportunity employment environment.