(Senior) Clinical Research Associate, IQVIA

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.

• →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

• 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