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# Senior Manager, Statistical Programming

- **Company:** Edetek Inc
- **Location:** United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Clinical Data Repository, Computer Programming, Databases, Unix Shell, SAP (Applications), SAS (Software), Enterprise Software Applications, Information Technology, Statistics Packages
- **Published:** October 29, 2026
- **Apply:** https://www.careerbuilder.com/job-details/senior-manager-statistical-programming--828603c6-9ced-4740-97bc-1360816179a4

## About the Role

Statistical Programming Languages, Statistical Programming Languages, Project/Program Management, Clinical Trial, Computer Programming, SAP, Statistics, Clinical Research, Graphics, Unix Shell Programming, * 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

## Description

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.