Senior Manager I, Clinical Data Standards & Reporting Engineer
Bristol Myers Squibb
Hyderabad, India
50% onsite
Clinical data standards
Cdisc standards
Sdtm mapping
This role is essential to the development and sustainability of Global & TA Clinical Standards that ensure compliant submissions and success of the BMS R&D pipeline
Job Summary
This role is essential to the development and sustainability of Global & TA Clinical Standards that ensure compliant submissions and success of the BMS R&D pipeline.
Responsibilities include serving as the primary point of contact for study teams on BMS standards, guiding interpretation and application, and acting as a consulting resource for validation of CDISC compliant submission packages.
The company offers a wide variety of competitive benefits, services, and programs that provide employees with the resources to pursue their goals, both at work and in their personal lives.
Matching Summary
This role is essential to the development and sustainability of Global & TA Clinical Standards that ensure compliant submissions and success of the BMS R&D pipeline.
Skills & Requirements
Must-have
Clinical Data Standards
CDISC standards
SDTM mapping
Medidata Rave
Metadata Repository
SAS & R coding
Nice-to-have
Life-changing careers
Balance and flexibility
High-achieving teams
Patient-focused innovation
Key Requirements
8 to 11 years of relevant industry experience
Bachelor's degree required
Experience with CDISC standards (USDM, CDASH, SDTM, ADaM)
Experience interpreting Health Authority regulations