Clinical Research Associate II, Oncology

Responsibilities

• Perform site monitoring visits including selection, initiation, monitoring, and close-out visits
• Ensure all activities comply with Good Clinical Practice (GCP) and ICH guidelines
• Work with sites to drive and track subject recruitment plans to enhance project predictability
• Administer protocol and study training to assigned sites and maintain regular communication
• Evaluate the quality and integrity of study site practices and escalate quality issues as needed
• Manage study progress by tracking regulatory submissions, recruitment, CRF completion, and data queries
• Create and maintain documentation including visit reports, follow-up letters, and action plans
• Collaborate with study team members to support project execution

Requirements

• At least 1 year of independent on-site monitoring experience for interventional studies in the UK
• Strong knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients
• Please note: This role is not eligible for UK visa sponsorship

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.