Senior Manager, Statistical Programming

The Senior Manager of Statistical Programming will stay hands-on with daily activities of a Statistical Programmer or Sr. Statistical Programmer. He/she

• Programs all tables, listings and graphs necessary for an assigned clinical study report (CSR);
• Acts as lead programmer for assigned projects;
• Programs customized data displays, (including data listings, summary tables and routine graphics) in accordance with the approved statistical analysis plan (SAP) and shell displays for clinical research studies;
• Writes code using Base SAS programs, SAS procedures, or standardized macros;
• Analyzes protocol, SAP, existing shells/templates as needed to understand structure and content of data;
• Performs data checks as needed, to ensure integrity and correctness of data displays;
• Prepares documentation for programs;
• Prepares documentation describing all datasets and variables within, including derived variables, and the project as a whole;
• Creates SAS datasets of clinical data from clinical databases;
• Creates status and efficacy datasets;
• Creates project-specific macros and formats;
• Loads client data from other platforms and other software packages;
• Prepares data to be sent to clients and as needed for other external transfers and data imports.

In addition to above job duties, Senior Manager of Statistical Programming also

• Communicates with clients to set and manage project timelines and deliverables;
• Assigns projects to the team and solves problems and/or technical difficulties;
• Trains junior team members on industry regulations, standards and internal tools used;
• Works with IT department to setup and ensure a secure environment with proper access control on SAS servers;
• Works with Quality Assurance team on Standard Operation Procedures drafting and revision, as well as testing and validation of CONFORM modules.

The Senior Manager of Statistical Programming will stay hands-on with daily activities of a Statistical Programmer or Sr. Statistical Programmer. He/shePrograms all tables, listings and graphs necessary for an assigned clinical study report (CSR); Acts...

• Ability to communicate effectively in English, in both writing and verbal.
• Ability to learn quickly and pay attention to details.
• Ability to manage multiple tasks/projects, effectively prioritize and execute tasks, and make quality and on time deliveries.
• Ability to work collaboratively, effectively, and productively in diverse organizational structures, and in interaction with dynamic clients.
• Ability to work independently, takes ownership and strives for quality and efficiency.
• Ability to work positively in a continually changing environment.
• Solid/Advanced SAS skills and understanding of the concept of standardization in data, programming, and statistical reporting of trial results and its implication to drug development.
• Master’s degree or above in Biostatistics, Computer Science, Mathematics, or a combination of education and relevant industry experience.
• Strong SAS programming language and good knowledge/experiences of clinical trial and drug development.
• At least 2 years of clinical SAS programming experience for the manager position.
• Some travel (5%) may be required with a potential of travel occurring over weekends.
• Cross-functional interactions

Note on Position Level:

We are open to considering qualified candidates at the Senior Manager, Associate Director, Director level, or above, depending on experience and qualifications.