As a Clinical Research Associate, you will oversee and coordinate clinical trials, ensuring compliance with regulations, collecting and analyzing data, and maintaining study documentation. Strong relationships with stakeholders and investigators are essential, along with an emphasis on patient safety and participation in study preparation.

Responsible for overseeing clinical trials, ensuring compliance with regulations, and collecting/analyzing critical data while coordinating study activities and maintaining documentation.

The Site Activation Lead oversees clinical trial start-up activities, manages site activation plans, leads communications, and ensures compliance with KPIs and regulations.

The Project Coordinator will support project management activities, coordinate documentation, assist with financial management, and ensure compliance with regulations.

The Safety Scientist will conduct safety surveillance, collaborate with teams for participant safety, and develop safety management plans in clinical research.

Oversees pharmacovigilance reporting activities, ensures compliance with regulatory requirements, enhances safety monitoring and manages reporting team.

The Clinical Research Associate conducts clinical trial activities including monitoring, data integrity checks, and collaboration with site staff while ensuring protocol compliance and patient safety.

The Study Start Up Associate will manage invoicing, client relationships, account reconciliation, and contract progression in clinical trials, ensuring timely billing and discrepancies resolution.

As a Senior Account Executive, you will generate new business for ICON Clinical Research, promoting services in pharmaceuticals and medical devices, while managing proposals and building relationships across the industry.

The TMF Specialist I will manage TMF documentation and compliance, contribute to contracts, organize documentation, and collaborate with teams to ensure accurate filing.

The Site Activation Lead will manage clinical trial start-up activities, ensuring projects meet client objectives and regulatory standards while overseeing site activation plans and team performance.

As an IHCRA intern at ICON, you will assist in planning and executing clinical trial activities, monitoring study progress, and ensuring compliance with protocols.

As an intern, you will support in-house clinical research activities, assist in managing clinical trials, and collaborate with team members to gain practical experience.

The Senior CRA oversees clinical trial activities ensuring compliance with protocols, manages multiple sites, monitors performance, and trains staff.

As Manager, Financial Business Partnering, you will provide financial insights to support various departments, manage budgeting and forecasting, conduct financial analyses, and present reports to stakeholders.

As a Pharmacovigilance Reporting Specialist, you will prepare safety reports, conduct data analysis, and ensure compliance with regulations while collaborating with teams.

As Director of Financial Business Partnering, you will drive financial strategy, collaborate with teams to optimize resources, and improve financial performance.

The Senior Manager, Financial Business Partnering provides strategic financial insights, collaborates on budgets and forecasts, analyzes financial performance, and develops a team of analysts.

The Senior Contract Analyst will manage contractual agreements, support project teams on compliance, and optimize contract management processes.

The Team Leader, IT Operations will manage IT operations, ensuring efficient technology service delivery, mentoring team members, and enhancing IT processes.