Description
The Senior Clinical Research Associate will lead clinical monitoring for designated projects, including planning and scheduling monitoring activities, overseeing CRAs and in-house personnel, developing CRA tools and training materials, managing visit reports and quality metrics, supporting risk planning and mitigation, maintaining the Trial Master File, and mentoring CRAs. The role requires at least eight years of CRA or relevant clinical research experience, prior Lead CRA experience, a bachelor's degree or equivalent qualification, hospital, pharmaceutical, or CRO study experience, and fluency in English. The employer offers hybrid work opportunities.
