Jobs at ICON plc

Lead the development and implementation of data science solutions for clinical trials, oversee programming activities, and ensure data integrity.

The Proposals Development Associate II supports business development by preparing client proposals and budgets for clinical trials, collaborating with cross-functional teams, and managing proposal workflows.

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

The Proposals Development Associate will lead client proposal preparation, collaborate with teams, conduct research, manage proposal workflows, and maintain proposal resources.

The role involves developing and validating statistical programs, analyzing clinical trial data, and collaborating with biostatisticians to ensure accurate reporting and compliance with regulations.

The Senior PK Scientist will author clinical pharmacology protocols, perform PK/PD analyses, develop analysis plans, and ensure compliance in clinical trials.

The Senior Account Executive will develop strategic relationships in pharma and biotech, identify business opportunities, and lead the full sales cycle for Imaging and Cardiac Safety solutions.

The Adjudication Project Manager manages endpoint adjudication processes for clinical trials, ensures project compliance, and leads study teams.

The Senior Director of Finance will oversee accounting and reporting, ensure compliance with US GAAP and IFRS, and guide financial strategy at ICON plc. Responsibilities include leading financial audits, managing complex accounting issues, and collaborating with other finance teams on strategic initiatives.

Lead the biostatistics consulting practice by providing statistical guidance, overseeing clinical trial design, and managing cross-functional teams for regulatory compliance and innovative solutions.

The PK Scientist will support protocol development, perform pharmacokinetic analyses, and collaborate on clinical pharmacology reporting in clinical trials.

Lead the creation and validation of SAS programs for statistical analysis, ensuring data integrity and collaboration with biostatisticians. Mentor junior programmers and contribute to regulatory submissions.

The Study Start Up Associate I manages site start-up activities, supports sites throughout project life, maintains qualification documentation, and communicates with various stakeholders.

As an IT Product Manager, you will oversee product lifecycle management, collaborating with stakeholders to implement and optimize IT products and services.

Manage global pharmaceutical supply and provide scientific, technical, and regulatory support for projects in Clinical Supplies. Oversee labeling, packaging, and distribution activities, and ensure compliance with regulatory requirements.

The Set Up Specialist coordinates the initial stages of clinical trials, ensuring compliance with regulations and supporting study teams throughout the setup process.

The Project Manager, IRT oversees IRT system activities, ensuring timelines and budgets are met, while managing stakeholder communications and risks.

As a Site Services Specialist I, you will provide logistical support to clinical trial sites, resolve site-related issues, and ensure compliance with protocols.

As a Project Manager in a laboratory, you will lead the management of clinical trials, ensuring adherence to regulations and maintaining client satisfaction while overseeing multiple ongoing studies.

The Principal Auditor in CRQA ensures quality and compliance of clinical trials, manages client relationships, and supports governance and risk management activities.