(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 company is seeking a Clinical Research Associate to lead site monitoring and support compliant, high-quality clinical trial execution. The role involves managing study progress, maintaining documentation, identifying risks, and collaborating with investigative sites and cross-functional teams.

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

• Make a direct impact on advancing clinical research and improving patient outcomes
• Work alongside experienced, collaborative teams
• Opportunities for growth and career development
• Incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to 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 Site Monitoring, Clinical Trial Management, ICH Guidelines, Protocol Compliance, Regulatory Compliance

Experience

• 1+ years