In-House Clinical Research Associate

Responsibilities

• Review and approve research and study regulatory documents for clinical trial implementation and monitoring
• Review clinical protocols to ensure data collection meets regulatory submission requirements
• Ensure monitoring activities are completed in accordance with company SOPs and Clinical Monitoring Plans
• Assist project managers with clinical study planning, management, and site training
• Develop and maintain relationships with clients, team members, and site personnel
• Assist in the identification and recruitment of potential investigators and study sites
• Maintain an accurate and complete Trial Master File throughout the project lifecycle
• Support site audits and site quality management activities

Requirements

• Bachelor’s degree in pharmacy, pharmaceutics, or a related scientific discipline
• 2+ years of clinical trial experience; monitoring experience is preferred
• Comprehensive knowledge of GCP and clinical monitoring procedures
• Experience using Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS)
• Proficiency in MS Office (Excel, Word, PowerPoint)
• Strong analytical, critical-thinking, and problem-solving skills
• Excellent written and verbal communication skills

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.