Associate Director, Biostatistics

Collaborates with cross-functional team to support observational studies Develops statistical sections of study protocols and statistical analysis plans. Collaborates with Data Management and Medical Research on design of eCRFs. Provides statistical guidance on conduct of ongoing studies. Contributes to observational study reports and regulatory documents, e.g., DSURs, briefing documents, etc. Contributes to scientific articles, summarizing data collected in Alnylam studies. Participates in other activities and meetings to support Biostatistics and the Medical Affairs team as needed. PhD in Biostatistics, Statistics, or equivalent with at least 6 years pharmaceutical biostatistics experience; or MS with at least 9 years' relevant experience. Excellent written and oral communication and presentation skills. Extensive experience and strong hand-on skills programming in SAS. Extensive experiences working on data analysis with clinical studies database Experience working on post-approval observational and clinical studies. Understanding of ICH GCP as well as general knowledge of industry practices and standards. Experiences in R programming language and other statistical software. Experience with CDISC, including SDTM, ADaM, CDASH.