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

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

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.

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

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

The Senior Financial Accountant will manage external reporting, monthly consolidations, and collaborate with finance teams to ensure accurate financial performance and compliance.

Conduct site visits for clinical trials ensuring compliance and data integrity while collaborating with investigators and preparing study documentation.

The Inside Sales Specialist I is responsible for identifying sales opportunities, engaging with clients, and managing sales pipelines while collaborating with the sales team.

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 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.

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

As a Senior Quality Assurance Auditor, you will perform audits for bioanalytical studies, ensuring compliance with regulations and facilitating client audits.

The Talent Acquisition Coordinator supports the recruitment process by scheduling interviews, managing candidate communications, and maintaining applicant tracking systems.

As a Pharmacovigilance Associate, you will manage medical information inquiries, assess adverse events, maintain databases, and support client projects.

The Clinical Research Associate II is responsible for site visits, ensuring compliance and data integrity throughout clinical trials, and contributing to study documentation.

Oversee and manage clinical trial activities ensuring compliance with regulatory standards, conduct site visits, and maintain data integrity.

Support the development and delivery of learning solutions at ICON, provide customer service via the LMS, and maintain training documentation.

As a Pharmacovigilance Assistant, you will support the collection, documentation, and reporting of safety data for medications and clinical trials, ensuring compliance with regulatory standards and contributing to patient safety. Your responsibilities include managing adverse event reports, data entry, safety report submissions, and maintaining records.

As a Site Contracts Negotiator, you will prepare, negotiate, and manage site contract agreements, ensuring compliance with ICON and client requirements, while maintaining communication with stakeholders.