Senior Clinical Research Associate - Lead Trials & Sites

Regulatory Toolkit; Durham (NC); On-site; USD 90,000 - 175,000; Full time

Job summary

IQVIA is seeking a Clinical Research Associate (CRA) to join our team in advancing clinical research. You will partner with investigative sites and cross-functional teams to drive site monitoring, ensure protocol compliance, and maintain data integrity, all while focusing on patient outcomes.

The position requires a life sciences-related bachelor's degree and 1.5+ years of on-site monitoring experience, with a strong grasp of GCP, ICH, and regulatory requirements.

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.

Responsibilities

• Lead and execute site monitoring visits (selection, initiation, routine, and close-out) per 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.

Skills

Communication

Problem solving

Organization

Education

Bachelor's degree in life sciences or related field

Job description

IQVIA is seeking a Clinical Research Associate (CRA) to join our team in advancing clinical research. You will partner with investigative sites and cross-functional teams to drive site monitoring, ensure protocol compliance, and maintain data integrity, all while focusing on patient outcomes.

The position requires a life sciences-related bachelor's degree and 1.5+ years of on-site monitoring experience, with a strong grasp of GCP, ICH, and regulatory requirements.