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As a Senior Clinical Research Associate, you will oversee clinical trial activities, ensuring compliance with protocols and regulatory requirements while managing site performance and collaborating with cross-functional teams.

As a Clinical Technology Specialist, you will lead the design and implementation of clinical systems, managing operations and ensuring compliance with regulations.

As a Global Study Manager at ICON, you will lead project management activities, develop plans, manage cross-functional teams, and ensure successful project execution.

The Global Study Manager will lead project management activities, develop plans, guide teams, and collaborate with stakeholders to achieve project goals in oncology clinical research.

The Global Study Manager oversees project management activities in oncology, ensuring successful project execution by leading teams, developing project plans, and maintaining stakeholder communication.

The Clinical Research Associate will conduct site visits for clinical trials, ensuring compliance and data integrity, and collaborating with site staff and investigators.

The Feasibility Principal Analyst leads the feasibility strategy for clinical studies, analyzes data for insights, mentors junior team members, and collaborates cross-functionally to optimize trial execution.

The Lead Clinical Research Associate will oversee clinical trial sites, manage site performance, mentor CRAs, and ensure compliance with regulatory standards.

Lead and oversee Phase I-II clinical trials as the Senior Principal Biostatistician, providing statistical input and mentoring junior statisticians.

The Global Study Manager oversees project management activities, leading teams to execute project plans, collaborating with stakeholders, and mentoring team members for successful project delivery.