Position Summary:

The Associate Director or Director, Statistical Programming is responsible for performing statistical programming activities in support of one or more clinical stage programs and/or studies.

Roles and Responsibilities of the Position:

• Perform data analysis using primarily the SAS programming language for the summary and interpretation of clinical trial data. 

• Implement and contribute to statistical analysis plans

• Perform data analysis, statistical analysis, generate safety and efficacy tables, listings and graphs

• Contribute to the development and review of CRFs, Data Management Plan, Data Validation Plan and edit check specifications. 

• Work cross functionally  to specify and perform ad hoc and prespecified analyses. 

Required Qualifications and Preferred Background:

Required:

• 7 years Pharmaceutical/Biotech programming experience is required.

• Expert proficiency in SAS Programming language is required. 

• Confident managing multiple projects.

• Strong communication skills 

• Strong well-rounded technical skills (EDC systems, MS Word, Excel, PowerPoint).
  
  Preferred:

• Experience with NDA submissions, integrated summaries (ISE/ISS) and Clinical Study Reports statistical deliverables is preferred.

• Experience in the analysis of complex oncology clinical trial data is preferred.

The base salary for the Assocaite Director level position could range from between $144,000 to $211,000, and the base salary for the Director level could range between $154,500 to $226,000. and will depend, in part, on the candidate’s qualifications for the role, including education and experience.