CRA II, Oncology

IQVIA seeks an experienced Clinical Research Associate for oncology site management in Manchester. The role involves conducting monitoring visits, managing recruitment, ensuring regulatory compliance, and coordinating with study sites across multiple protocols.

Responsibilities

• Conduct site selection, initiation, monitoring, and close-out visits per GCP and ICH standards
• Collaborate with sites to develop and track subject recruitment plans
• Deliver protocol training and maintain regular communication with assigned sites
• Evaluate site compliance with protocol requirements and regulatory standards
• Track study progress including regulatory submissions, enrollment, CRF completion, and data queries

Requirements

• Independent on-site monitoring experience
• Track record managing multiple clinical trial protocols at diverse sites
• In-depth knowledge of GCP and ICH guidelines
• Life science degree or equivalent industry experience
• Flexibility to travel to study sites