Responsible for all statistical tasks on the assigned clinical trials, and perform these tasks with a high level of independence ?Responsible for all statistical tasks on the assigned clinical trials, and perform these tasks with a high level of independence. For example, clinical trial design/planning, regulatory interactions, analysis plan, reporting activities, CTD and summary documents, exploratory analyses, and statistical consultation. ? May be assigned to lead a small project or parts (e.g., indication(s)) of a project, initially under the supervision/guidance of a more experienced statistician but with increasing autonomy and accountability. ? Track clinical trial/allocated project activities and milestones. ? Interact with the Novartis Method group as appropriate. ? Ensure timelines and adequate quality of all Biostatistics and Statistical Reporting (B&SR) deliverables for the assigned trials and project tasks. ? Follow processes and adhere to Novartis and project specific standards as well as Health Authority requirements (SOPs, Master Analysis Plan, full development project specifications, and regulatory guidelines). ? Establish and maintain sound working relationships and effective communication within the Clinical Trial Team and B&SR team. ? Participate in or lead non-clinical project activities as needed"
PhD in Statistics or Masters Degree in Statistics (or equivalent degree) English PhD in Statistics with at least 0-3 years of pharmaceutical experience
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