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.
The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or any other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, marital or veteran status, disability, or any other legally protected status.
PhD in Statistics or Master s Degree in Statistics (or equivalent degree. English. 5+ years of pharmaceutical experience.
candidates with PhD will be given priority consideration
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