Hybrid Senior Statistical Programmer Analyst bei Janssen Research & Development

Sr. StatisticalProgrammer Analyst – Janssen

Janssen Research &Development, a member of Johnson & Johnson's Family of Companies, isrecruiting for a Sr. Statistical Programmer Analyst. 

At the JanssenPharmaceutical Companies of Johnson & Johnson, what matters most is helpingpeople live full and healthy lives. We focus on treating, curing and preventingsome of the most devastating and complex diseases of our time. And we pursuethe most promising science, wherever it might be found.

Janssen Research &Development discovers and develops innovative medical solutions to addressimportant unmet medical needs in oncology, immunology, neuroscience, infectiousdiseases and vaccines, and cardiovascular and metabolic diseases. Please visithttp://www.JanssenRnD.com for more information.

We are Janssen. Ourmission drives us. Our patients inspire us. We collaborate with the world forthe health of everyone in it.

The Sr. StatisticalProgrammer Analyst is an individual contributor in the Statistical Programming and AnalysisDepartment, that will be accountable for development, verification, anddocumentation of SAS code on the assigned clinical project.  This role isthat of a SAS programmer who is capable of supporting programming requests of mediumto high complexity in support of clinical trial reporting and submissions, withminimal guidance. 

Principalresponsibilities will include:

• Design and development of statistical programs for the assigned project
• Perform quality control in support of clinical R&D analysis and reporting
• Maintain documentation as appropriate
• Completes programming tasks of medium to high complexity
• Critically reviews requirements and data, identifies gaps, suggests solutions and applies expertise on clinical R&D statistical programming activities.

Qualifications:

• A Bachelor’s degree or higher in Computer Science, Mathematics or other scientific fields is required
• In-depth knowledge of SAS statistical software with a minimum of 5 years SAS programming experience with increasing responsibility is required
• Knowledge of SAS macro language and SAS Graph is desired
• Experience in a pharmaceutical/clinical trial environment is preferred.
• Demonstrated written and verbal communications skill is required.
• Experience working with programmers in a team environment is preferred.
• Prior experience with any of the following Therapeutic Areas is preferred: Oncology, Neuroscience, Immunology, Cardiovascular, Metabolics, Infectious Diseases and Vaccines.
• Knowledge and experience in SDTM and ADaM is required
• A working knowledge of Statistics is required

We are an equal opportunityemployer and value diversity at our company. We do not discriminate on thebasis of race, religion, color, national origin, gender, sexual orientation,age, marital status, veteran status, or disability status.