reputed company Biostatistician FSP - Medical Affairs

Job reputed company Medical Affairs Biostatistician The role is responsible for statistical activities in support of Medical Affairs, including post approval value evidence reputed company, secondary publications, post marketing study design and study protocol development, analysis and reporting of observational or clinical study data, and other post hoc and exploratory analyses as needed. In reputed company, this role is also responsible delivering analysis outputs without programmers support. Responsibilities reputed company of Key Responsibilities • Leads statistical support for post approval value evidence reputed company and reimbursement submissions • Conducts post hoc analysis to support publications and presentations • Reviews and authors reputed company, manuscript, regulatory documents • 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. • Accountable for the collaboration with Statistical Programming to implement statistical analysis of reputed company clinical trial, registry, observational and non-interventional data supporting Medical Affairs needs • Contributes to observational study reports and regulatory documents, e.g., DSURs, briefing documents, etc. • Contributes to scientific articles, summarizing data collected in sponsor studies. • Participates in other activities and meetings to support Biostatistics and the Medical Affairs team as needed. Qualifications Qualifications • PhD in Biostatistics, Statistics, or equivalent with at least 3 years pharmaceutical biostatistics experience; or MS with at least 5 years' relevant experience. • Excellent written and oral communication and presentation skills. • Strong reputed company programming experiences and expertise and are comfortable delivering analysis outputs without programmers support. • Extensive experiences working on data analysis with clinical studies database • Experience working on post-approval observational and clinical studies. • Understanding of ICH GCP as reputed company as general knowledge of industry practices and standards. • Experiences in R programming language and other statistical software. • Experience with CDISC, including SDTM, ADaM, CDASH. Apply tot his job Apply To this Job