's or master's degree in health and/or pharmaceutical sciences, physical/biological, or chemistry fields. At least 5 years...
Responsibilities: Attending multi-disciplinary team meetings, representing the programming function. Create or review and approve programming plans at study and project level. Provide input on key study-related documents produced by oth...
Responsibilities: The Senior Statistical Programmer I will assist the US and/or EU Early Phase Statistical Programming teams by developing SAS programs for analysis datasets. They will be responsible for listing and safety summary tables...
Responsibilities: Participate in developing and maintaining clinical trial data and statistical programming standards to ensure the company standards are up to date and in line with pharmaceutical industry standards, conventions, and regu...
Responsibilities: Lead projects with higher level of complexity/challenges/difficulties. Lead efforts to resolve complex statistical programming issues or problems. Perform a leadership role in statistical programming projects by coordi...
Responsibilities: Cleaning and transforming raw clinical trial data from various sources to ensure accuracy and consistency for PK/PD analysis. Writing SAS code to perform descriptive analysis of PK/PD data and statistical analysis of ex...