Clinical Research Associate, Sponsor Dedicated

Location: Durham, North Carolina, United States; candidates must reside in the United States

Salary: $71,900–$189,000 annualized base pay

Company

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

What you will do

• Perform site selection, initiation, monitoring, and close-out visits in accordance with the study protocol, Good Clinical Practice, and applicable regulations.
• Support subject recruitment plans and track recruitment, enrollment, regulatory submissions, approvals, and data query resolution.
• Train assigned sites on study protocols and maintain regular communication to manage project expectations and issues.
• Evaluate site practices, identify quality issues, and escalate deviations when appropriate.
• Maintain Trial Master File and Investigator Site File documentation, visit reports, follow-up letters, and action plans.
• Collaborate with study teams and support site financial management and invoice retrieval when applicable.

Requirements

• Bachelor’s degree in a scientific or healthcare discipline preferred; equivalent education, training, and experience may be accepted.
• At least 2 years of on-site monitoring experience.
• Knowledge of clinical research regulations, Good Clinical Practice, and International Conference on Harmonization guidelines.
• Good therapeutic and protocol knowledge, with proficiency in Microsoft Word, Excel, PowerPoint, and relevant mobile devices.
• Good command of written and verbal English is required.
• Strong communication, organizational, problem-solving, time-management, and financial-management skills.

Culture & Benefits

• Full-time employment with base pay determined by qualifications, experience, location, and schedule.
• Potential incentive plans, bonuses, health and welfare benefits, and other benefits may be available.
• Equal opportunity employment committed to a fair and inclusive hiring process.