Jobs at ICON plc

The Clinical Quality Compliance Lead oversees quality assurance in clinical trials, ensuring compliance with regulations and standards while leading audits and cross-functional collaboration.

The Clinical Training Development Lead develops innovative training programs, manages courseware development, evaluates program effectiveness, and ensures compliance with training regulations.

As a Proposals Writer II, you will develop client-ready proposals, collaborate with experts, and manage project timelines in clinical research.

As Director of Clinical Operations, you will oversee clinical trial planning and execution, ensuring compliance, quality, and optimized outcomes through team collaboration and strategic direction.

The Manager oversees contracts management, negotiating agreements, ensuring compliance, and supporting project teams with contract-related issues.

As a CRA, you will monitor clinical trials, coordinate activities, maintain documentation, and ensure compliance with safety and regulatory standards.

Manage and coordinate post-trial access programs. Ensure timely delivery within budget, lead cross-functional teams, and develop strategic plans for investigational products.

The Operations Quality Specialist provides support to Clinical Research Associates, ensuring protocol compliance, managing investigational sites, and tracking study data and documentation while assisting with site training and audits.

The Operations Quality Specialist ensures compliance with regulatory standards through quality assessments, process improvement, incident management, and staff training in quality assurance protocols.