Support RWDS project teams and be accountable to the project manager/director for those projects
Summarize and synthesize a wide range of medical and statistical information, including disease specific and pharmaceutical product research
Develop an understanding of Regulatory/HTA requirements for RWE, at least in the European and/or North American context
Support development of study documents (eg. protocols, analysis plans, reports, posters, manuscripts) under guidance from scientific team members and project manager/s
Liaise and manage processes with ethics committees, application committees and other relevant stakeholders to support acquisition of data for studies
Interpret and communicate the results of clinical/observational studies, health economic models (cost-effectiveness and budget impact) and statistical analyses
Undertake primary and secondary research initiatives including the retrieval and analysis of data, competitive product pipeline information, epidemiology trends, etc. according to needs of the project
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