Clinical Research Associate I
Maidenhead, England, United Kingdom · Full Time
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- Experience
- Any
- Salary
- —
- Openings
- 1
- Posted
- 3 weeks ago
- Work mode
- In office
- Resume
- Required to apply
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Job description
About the Role
Join a dynamic Clinical Operations team based in the UK focused on multi-sponsor projects, offering an engaging CRA I position for candidates with a minimum of six months’ independent monitoring experience. The role provides exposure across varied therapeutic areas such as Hematology/Oncology and Ophthalmology, participating in innovative clinical trials within a thriving global CRO.
Key Responsibilities
- Perform monitoring activities nationally across clinical sites in the UK.
- Focus primarily on oncology studies involving solid tumors, including Prostate, Non-Small Cell Lung Cancer (NSCLC), Leukemia, Breast cancer, Glioblastoma, and various hematological malignancies.
- Manage multiple study protocols in therapeutic domains including Neuroscience, Cell and Gene Therapies, Respiratory, Cardiovascular, Infectious Diseases, Nephrology, Endocrinology, and Gastroenterology.
- Implement risk-based monitoring approaches to optimize trial oversight and management efficiency.
- Conduct at least eight days of on-site visits monthly to support study progress and compliance.
Professional Development and Culture
- Access personalized career development plans and opportunities for progression within the company.
- Experience a supportive work environment with flexible and approachable management.
- Engage in collaborative projects with leading biotech and biopharmaceutical innovators.
Equal Employment Opportunity
The company is committed to fairness in employment practices and provides accommodations as necessary to support diverse applicant needs.