CRA II, Oncology

Overview

Join IQVIA as a Clinical Research Associate to advance clinical trials and patient outcomes. You will combine on-site and remote monitoring to support site performance within GCP and ICH guidelines. You will train sites, manage recruitment plans, and ensure quality and regulatory compliance. You will track study progress, handle documentation in TMF/ISF, and collaborate with the study team to keep projects on schedule. This role offers exposure to cutting-edge medicines and career development within a global leader in clinical research.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with GCP and ICH
• Drive and track subject recruitment plan aligned with project needs
• Administer protocol training to sites and maintain regular communication
• Evaluate site practices for protocol conduct and regulatory adherence; escalate issues as needed
• Track regulatory submissions, recruitment, CRF completion, data queries; support start-up phase
• Ensure site documents are filed in TMF and ISF maintained per GCP/regulations
• Create and maintain documentation on site management, visit findings, and action plans
• Collaborate with study team members for project execution support

Key requirements

• Experience of independent on-site monitoring with GCP, protocol requirements, and regulatory guidelines
• Managed multiple clinical trial protocols across diverse investigative sites
• Hands-on experience in the Oncology therapeutic area
• Flexibility and commitment to nationwide travel

• strong communication
• collaboration
• problem solving
• GCP compliance
• ICH guidelines
• regulatory submissions and approvals

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