(Senior) Clinical Research Associate

IQVIA is a global provider of clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries. The Clinical Research Associate will monitor clinical trial sites, ensure protocol compliance and data integrity, manage study progress, address risks, and collaborate with cross-functional teams to support successful study delivery.

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

Benefits

• Opportunities for growth and career development
• Incentive plans, bonuses, and/or other forms of compensation may be offered
• A range of health and welfare and/or other benefits

Company

• Clinical research, commercial insights, and healthcare intelligence for life sciences.
• Durham, North Carolina, USA
• https://www.iqvia.com/
• Founded in 1982
• 10001+ employees

Qualifications

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

Required skills

• Clinical Trial Regulatory Requirements, ICH Guidelines

Experience

• 1+ years