This position will serve as a Study Associate (CR), playing a key role in the design of Castle-sponsored clinical studies and the development and management of study-related case report forms (CRFs). The Study Associate will ensure the thorough maintenance, review, and transition of clinical data from the CRF to the R&D team. This role will collaborate with colleagues across Clinical Research, IT, and R&D to support CRF development and contribute to data integrity through quality reviews and validation activities following data transfer. The Study Associate will also participate in study design and protocol development and is expected to develop and maintain therapeutic area expertise across Castle's diverse clinical portfolio to support successful study execution.
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Job Type
Full-time
Career Level
Mid Level