About the role
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 skillsA 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.
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JOB OVERVIEW
Experience level
Senior
Location
Denver, CO
Occupation
Clinical Research Coordinators
Industry
Other Scientific and Technical Consulting Services
Posted
3 days ago
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