Hiring: Study Start-Up CRA (FSP) | UK I'm currently supporting a CRO in the search for a Study Start-Up CRA to join a dedicated Functional Service Provider (FSP) model. This is an excellent opportunity to work on innovative clinical development programmes within a highly collaborative and quality-driven environment. Key Responsibilities: • Lead and coordinate study start-up activities across the UK • Prepare and submit regulatory and ethics applications (IRAS, HRA, MHRA, REC) • Support site identification, feasibility, activation, and initiation activities • Ensure timely collection and review of essential regulatory documentation • Collaborate with Clinical Operations, Regulatory Affairs, and site teams to meet study timelines • Track start-up milestones and proactively identify and resolve issues • Maintain compliance with ICH-GCP, local regulations, and sponsor procedures What We're Looking For: • Previous experience in Clinical Research, Study Start-Up, Site Activation, or CRA roles • Hands-on experience with UK submissions, including IRAS, HRA, MHRA, and REC processes • Strong understanding of clinical trial regulations and study start-up activities • Experience working within a CRO, pharmaceutical company, or FSP environment • Excellent stakeholder management and communication skills • Ability to manage multiple studies and priorities simultaneously What's on Offer: • Opportunity to support a world-class clinical development portfolio • Exposure to cutting-edge therapies across multiple therapeutic areas • Flexible working environment • Strong career development and progression opportunities • Collaborative international team culture If you have experience in UK study start-up and are interested in learning more, I'd be happy to arrange a confidential discussion.
