Clinical Research Associate II/ Senior Clinical Research Associate

About This Role

This night-shift post on the cardiac ward pairs patient care with mentoring new nurses. At Fortrea Clinical Pharmacology Services in Leeds, Clinical Research Associates (CRAs) are on site, in the flow of the study, when it matters most. You will see dosing days, walk the clinic floor, and review data as it is generated, not months later. This is a full-time, permanent job supporting Phase I–Ib studies.

Responsibilities

• Monitor Phase I–Ib studies across Fortrea Clinical Research Unit (CRU) and selected UK sites
• Perform Process Monitoring, Pre-Study, Site Initiation, Routine Monitoring, and Close-out visits
• Review source data, protocol compliance, and data quality using modern eSource and EDC systems
• Collaborate closely with clinical, lab, and project teams during fast-paced study timelines

Requirements

• Minimum 2 years independent site management monitoring experience (including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring and Close-Out Visits) according to monitoring plan requirements, SOPs and ICH GCP guidelines
• Life science degree or nursing qualification
• Independently eligible to work in the UK

Benefits

• Car allowance
• Flexible working arrangements
• Exposure to early-phase science that accelerates CRA development
• Collaborative team environment based in a modern Leeds CRU
• Access to innovative clinical trials technology
• Remote working when not monitoring

Important Details

• Work format: remote working when not monitoring, with option to work from the office

About the Company

Fortrea Clinical Pharmacology Services operates a world-class 100-bed, 65,000 ft² Clinical Research Unit in Leeds, where life-saving medicines begin their journey.