The Senior Regulatory Affairs Specialist will oversee product registrations, ensure regulatory compliance, maintain licenses, and collaborate on regulatory submissions and intelligence within health authorities.

As an Intern at ICON, you will assist with research, data collection, support project initiatives, prepare reports, and engage in professional development.

As a Client Services Associate I, you will manage client relationships, address inquiries, coordinate meetings, and provide administrative support to ensure client satisfaction and project execution.

As an Intern, you will support various projects by assisting with research, data analysis, preparation of reports, and daily administrative tasks.

The Intern will assist in research, data collection, and administrative tasks, develop skills, and support team projects and operations.

As an Intern, you will assist with research, data collection, and analysis while supporting various projects, enhancing workflows, and engaging in professional development activities.

The Senior Manager, FSA leads a team of Site Contracts Negotiators to ensure efficient contract management and compliance in clinical trials.

The Clinical Trial Administrator supports clinical trial coordination, documentation management, communication with teams, and tracking clinical metrics while ensuring compliance with protocols and regulations.

The role involves supporting clinical trials by ensuring compliance with regulations, maintaining data accuracy, managing contacts, and assisting with investigator recruitment. Strong communication and organization skills are necessary, along with a commitment to team collaboration.

The Graduate Pharmacovigilance Associate supports safety monitoring of pharmaceutical products, assisting with data collection, report preparation, and documentation compliance.

Lead and develop the financial reporting team, ensuring compliance with US GAAP and local legislative requirements while managing monthly accounts and audits.

The Site Contracts Lead will manage the development and execution of site agreements for clinical trials, liaise with teams and clients, and ensure contract compliance.

The Senior Clinical Data Coordinator will manage data for clinical trials, ensuring quality and regulatory compliance, and mentor junior coordinators.

Responsible for negotiating and maintaining clinical trial agreements, ensuring compliance and effective communication with study sites and stakeholders. Must draft, review, and manage contractual documents, track progress, and adhere to departmental guidelines.

As a Project Manager, you will lead the delivery of Firecrest projects, ensuring timely execution, coordinating teams, managing risks, and communicating progress to stakeholders.

The Clinical Research Associate oversees clinical trials, ensuring compliance with regulations and maintaining study documentation, while developing strong stakeholder relationships and ensuring patient safety.

The Study Start Up Associate I will assist in preparing regulatory documents, coordinating approvals, maintaining records, and supporting study teams in clinical trials.

As a Senior Clinical Data Science Programmer, you will develop programming solutions for clinical trial data analysis, collaborate with scientists, and ensure data quality for regulatory submissions.

As a Senior Statistical Programmer, you will build and validate statistical programs, lead programming deliverables, and ensure compliance with global trial regulations.

The Principal Biostatistician will lead statistical activities for clinical trials, analyze complex data, and collaborate with teams on study design and regulatory submissions.