CRA 2/Senior CRA 1

About the role

We’re looking for a passionate and driven Clinical Research Associate (CRA) to join our team and play a key role in delivering high-quality clinical trials. In this role, you’ll partner with investigative sites and cross-functional teams to ensure studies are executed with excellence, compliance, and patient focus.

Responsibilities

• Lead and execute site monitoring visits (selection, initiation, routine, and close-out) in accordance with GCP/ICH guidelines
• Build strong relationships with investigative sites to drive performance, recruitment, and engagement
• Ensure protocol compliance, data integrity, and high-quality study execution
• Proactively identify risks, resolve issues, and escalate when needed
• Track and manage study progress, including regulatory approvals, enrollment, and data quality
• Maintain accurate documentation and contribute to inspection readiness
• Collaborate with cross-functional teams to ensure successful study delivery

Requirements

• Bachelor’s degree in life sciences, healthcare, or related field (or equivalent experience)
• 1.5+ years of on-site monitoring experience
• Solid understanding of GCP, ICH, and regulatory requirements
• Strong communication, problem-solving, and organizational skills

Qualifications

• Ability to manage multiple priorities in a fast-paced environment

Skills

• Effective communication and collaboration skills
• Proficiency in relevant software tools

Benefits

• Make a direct impact on advancing clinical research and improving patient outcomes
• Work alongside experienced, collaborative teams
• Opportunities for growth and career development
• Dynamic, fast-paced environment where your contributions matter

Pay

The potential base pay range for this role, when annualized, is $90,200.00 - $175,100.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).

Schedule

Field-based

Location

Chicago, United States of America

IQVIA is an Equal Opportunity Employer

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.

Learn more

To learn more about this exciting opportunity, visit IQVIA's careers page.