Description
Accountable for:
· Apply knowledge of basic and complex statistical design, analysis, and programming techniques
· Efficiently and effectively coordinate statistical activities for multiple projects simultaneously.
· Serve as primary statistical representative for biometrics standalone projects or otherwise complex studies.
· Effectively manage broad based projects such as NDA submissions or complex, multi-protocol programs, potentially coordinating activities across multiple locations
· Maintain awareness of project budgets and tasks, and effectively communicate the status of such tasks to line management and the project manager, as appropriate
· Actively monitor project budgets and help staff identify resource or scope of work changes.
· Interact with project team and line manager to identify project priorities and communicate such activities and associated timelines to departmental management
Qualifications/ Requirements:
· Master’s degree, equivalent, or higher in Biostatistics or related field
· 6+ years of Industry experience
· Experience with Bayesian analysis preferred
· Ability to write code to validate efficacy outputs required
· Excellent communications skills (written and spoken) for both internal and external communications.
· Experience with regulatory submissions and support preferred
· Ability to maintain confidentiality of data and information during interactions with staff at all levels
· Extensive experience in leading statistical activities in clinical research
· Ability to program in one or more statistical software packages used to conduct statistical analyses
· Proven ability to effectively communicate statistical concepts
· You must have previous experience in either a biotech, CRO or pharma company
For a confidential discussion please contact
Jonathan Cunliffe at Umbilical on
+49 3221 421 9777 or email Jonathan@umbilical-life.com