Senior Manager, Clinical Data Standards & Reporting Engineer

Bristol Myers Squibb is seeking a Senior Manager, Clinical Data Standards & Reporting Engineer to lead the development and sustainability of global and TA clinical standards. The role will report to the Associate Director, Clinical Data Standards & Reporting. The successful candidate will have 8-11 years of experience in clinical trials, preferably with clinical data standards as a focus, and experience in industry standards such as CDISC, Medidata Rave, and Metadata Repository.

Requirements

• Serve as the primary point of contact for study teams on the usage and development of BMS standards
• Guide study teams in interpreting and applying end-to-end standards for implementation into a clinical trial
• Participate in relevant study team meetings as a Standards SME and provide interpretation and rationale for standards components
• Act as a consulting resource for study team members regarding the validation of the CDISC compliant submission packages and relevant submission documents
• Develop training materials and provide training on clinical data standards and reporting developed processes

Benefits

• Competitive benefits and services
• Wide variety of benefits and programs
• Resources to pursue goals, both at work and in personal lives