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:
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.
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