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The role includes the completion of clinical trials, to both the assigned time frames and appropriate quality standard, as well as presenting the results at conferences and external non-study meetings. Alongside leveraging local regulatory and therapeutic expertise across areas such as oncology, cardiology, metabolic disease, central nervous system, anti-viral and anti-infective.
*Contribution to clinical development of plan preparation
*Develop detailed data analysis plans for various projects
*Programming of study analysis, including review of results and preparation of statistical methods for reporting.
*Communication of project requirements for CRF design, database clean-up and design, ensuring the key variables are suitable for analysis.
*Communicate clearly statistical results to medical writing personnel to ensure an accurate interpretation of key findings.
*Ph.D. Biostatistics/ Statistics, with strong experience in SAS programming or equivalent.
*Knowledge of advanced statistical methods and regulatory requirements/guidelines for drug development.
*Knowledge of pharmaceutical industry
*Previous experience working in a pharmaceutical or CRO setting is desirable.