We are partnering with a leading CRO to appoint a Clinical Research Associate II to support the delivery of high-quality clinical trials. This is an excellent opportunity for a CRA with monitoring experience who is looking to further develop their career within a collaborative and fast-paced environment. You will be responsible for conducting on-site and remote monitoring visits, ensuring studies are delivered in accordance with protocols, ICH-GCP, SOPs, and applicable regulatory requirements, while working closely with investigative sites and cross-functional project teams.
Key Requirements:- Bachelor's degree in a scientific discipline (or equivalent experience)1–2 years' clinical monitoring experience across on-site and remote studies
- Good understanding of ICH-GCP and clinical research regulations
- Experience conducting monitoring visits and managing site activities
- Strong organisational, communication, and problem-solving skills
- A proactive, detail-oriented approach with the ability to work independently and collaboratively
If you're looking to join a growing organisation where you'll gain exposure to a diverse range of clinical studies and continue developing your CRA career, I'd love to hear from you.
