Statistical Trial Analysis
Collaborate with other statistical colleagues and study personnel to provide input to statistical analysis plans.
Assist in and/or be accountable for selecting statistical methods for data analysis, authoring the corresponding sections of the data analysis plan, and conducting the actual analysis once a reporting database is
Collaborate with data management in the planning and implementation of data quality assurance
Maintain proficiency with respect to SAS programming and statistical methodology and in applying new and varied methods.
Effectivel y justify methods selected and implement previously outlined analysis plans.
Conduct peer-review of work products from statistical
Effectively utilize current technologies and available tools for conducting the clinical trial
Communication of Results and Inferences
Collaborate with other statistical colleagues to write reports and communicate
Responsible for assisting in the communication of study results via regulatory submissions, and manuscripts, as well as for communicating one-on-one with key
Assist or respond to regulatory queries working in collaboration with other statistical
Therapeutic Area and Systems Knowledge
Understand relevant disease states in order to enhance the level of customer focus and
Ensure replication of tools and systems, where applicable and stay informed of technology
Regulatory Compliance
Perform work in full compliance with assigned curriculum(s) and will be responsible for following applicable Corporate, Medical, local, and departmental policies, procedures, processes and
Education Qualification
Bachelors Degree is the minimum requirement for this role .
