Clinical Research Associate

Responsibilities

• Perform site monitoring visits, including selection, initiation, monitoring, and close-out visits
• Ensure clinical studies comply with study protocols, applicable regulations, and sponsor requirements
• Work with sites to drive and track subject recruitment plans to enhance project predictability
• Administer protocol and related study training to assigned sites
• Evaluate the quality and integrity of study site practices and escalate quality issues as appropriate
• Manage study progress by tracking regulatory submissions, recruitment, and data query resolution
• Maintain appropriate documentation regarding site management and monitoring findings in the Trial Master File (TMF)
• Collaborate with study team members to support project execution

Requirements

• Bachelor's Degree in a scientific or healthcare discipline (or an equivalent combination of education and experience)
• At least 1 year of on-site monitoring experience
• Strong knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Proficiency in Microsoft Office (Word, Excel, and PowerPoint)
• Excellent written and verbal communication skills in English
• Strong organizational, problem-solving, and time management 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.