Top Tech Jobs & Startup Jobs in Dublin

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.