Bristol Myers Squibb Principal Analyst in Pennington, New Jersey

Title: Principal Analyst

Location: NA-US-NJ-Pennington

Job Number: 1702110

Employer: Bristol-Myers Squibb Company

Position: Principal Analyst I (ref.# 9561)

Location: 311 Pennington-Rocky Hill Road, Pennington, NJ 08534

Duties: Draw on experience/skills with programming using SAS software, authoring specifications, knowledge of pharmaceutical drug development process, clinical trial, and regulations related to pharmaceutical drug development to provide comprehensive programming support for project teams, including development of programming strategies, standards, specifications and programmed analysis. Support the development of strategies and technologies for flexible and global clinical trial programming. Create datasets, tables, listings and graphs, using SAS Software, for various regulatory requirements in support of clinical trials. Modify, enhance and troubleshoot existing SAS code and SAS Macro code to produce outputs. Create and modify SAS programs for the purposes of validating outputs created by others. Communicate effectively with departmental project and functional leadership concerning project issues including data, technical and timelines. Ensure alignment with Planning & Execution Lead with regard to priorities and scope of work assignments. Proactively, inform Planning & Execution Lead of issues/risks to the project and potential remediations. Review key planning documents including statistical analysis plan, data presentation plan and data review plan to ensure alignment with development team objectives and clarity and completeness of programming assumptions and requirements. Support the development of unambiguous and robust programming specifications for internal and external programming work. Interact with vendors regarding project standards, programming conventions, programming specifications and file transfers. Provide technical guidance to vendors supporting analysis and reporting work. Provides support for acceptance of vendor deliverables. Build successful partnerships and seamless interfaces within department and the broader organization. Provide timely and effective communication to project team members, highlighting department goals and priorities, ensuring work efforts parallel departmental objectives. Ensure quality of department deliverables by consistently applying analysis and reporting standards and complying with regulatory requirements, guidance and corporate and departmental Standard Operating Procedures and work practices. Identify opportunities for increased efficiency and consistency within a project team. Contribute to improvement and standardization of processes, standards and tools.

Requirements: Bachelor’s degree (or foreign equivalent) in Chemistry, Industrial Biotechnology, Statistics, Computer Science, Life Sciences, Physics, Mathematics or a related field plus 5 years of post-baccalaureate clinical/statistical programming experience within pharmaceutical clinical development and experience reflecting demonstrable ability in the skill set described above.

* This position is eligible for our employee referral program

Contact: Raveena Gayo

1 Squibb Drive

Princeton, NJ 08540

resume.com@bms.com

Bristol-Myers Squibb is an equal opportunity employer - Minorities/Females/Protected Veterans/Disabled

Job: Biostat - Programming