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Conduct national monitoring across the UK for a diverse range of therapeutic areas including oncology and ophthalmology. Manage clinical trials using a risk-based monitoring model to ensure efficient trial oversight.
Our Clinical Operations (multi-sponsor) team in the UK is looking for a passionate CRA I with at least 6 months of independent monitoring experience to work across a diverse range of therapeutic areas – including Hematology/Oncology and Ophthalmology. This is your chance to gain hands-on experience in groundbreaking clinical trials while being part of a supportive, fast-paced and innovative global CRO.
✅ National monitoring across the UK
✅ Oncology focus, including solid tumor studies, Prostate, NSCLC, Leukemia, Breast, Glioblastoma & Hematological Malignancies
✅ Exposure to multiple protocols across Neuroscience, Cell/Gene Therapies, Respiratory, Cardiovascular, Infectious Disease, Nephrology, Endocrinology & Gastroenterology
✅ Risk-based monitoring model for smarter trial management
✅ 8+ on-site days per month
At our global CRO, we blend 30 years of expertise with innovation, offering:
🌟 Personalized development plans & career progression
🌟 A supportive environment with flexible Line Managers
🌟 Exciting collaborations with biotech & biopharma pioneers
Make a real impact in clinical research while building your career with a company that invests in your growth and success!
Ready to make a difference? Let’s connect!
Learn more about our EEO & Accommodations request here.
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