Clinical Research Associate

Responsibilities

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

Requirements

• Bachelor’s degree in life sciences, healthcare, or a related field
• 1+ year of onsite monitoring experience
• Proven experience in oncology monitoring
• 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

About the Company

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.