Teva R&D Programmer IV 

India, Karnataka, Bengaluru 

79949301

The Clinical Programming Manager is responsible for managing the timely and accurate execution of programming components of clinical trials.

The Manager leads and manages completed projects that involve global tasks, cross functional teams, or outsourcing resources. The role may require providing input to design and analysis, and report the results of clinical trials, including programming rules and mocked T/L/G. In addition, providing all safety claims for new drugs and extension of claims/publication support for our marketed drugs.

• Provides input for Budget Planning
• Likely to oversee contingent workers and/or vendors; Likely to provide training to others
• Primarily works at the project level
• Delivers assignments with quality and within timelines
• Contributes strategy under moderate supervision
• Provides strong programming support to CDISC based e-submission. Develop, review, and/or perform validation of generic macros. Develop, debug, and enhance SAS programs to support quality control of safety or efficacy derived datasets
• Has good knowledge and understanding of the statistical models in efficacy data analysis
• Responsible for the standardization of Clinical Programming deliverables within a project
• Extends existing or develops new clinical programming methods to solve complex problems

• Bachelor’s Degree/ Master’s Degree/ PhD in Science, Statistics, Information Technology or equivalent combination of education and related work experience.

• Bachelor’s + 5 years or Master’s + 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer

• Experience in SDTM and ADaM acquainted with CDISC Guidelines and requirements.