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Teva Pharmaceuticals logo

R&D Programmer III

2 - 6 years

0 Lacs

karnataka

Posted:5 days ago| Platform: Shine logo

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Skills Required

sas programming sdtm adam clinical programming cdisc guidelines

Work Mode

On-site

Job Type

Full Time

Job Description

The R&D Programmer III position at Teva Pharmaceuticals in Bangalore, India offers an exciting opportunity for a Senior Clinical Programmer to support clinical projects and regulatory submissions. As part of a global team dedicated to making good health more affordable and accessible, you will play a lead role in generating and validating analysis datasets, tables, listings, and figures. Your expertise in SAS programming will be crucial in developing global data standards, including SDTM, ADaM, and Teva's database structure. Your responsibilities will include working at the project level, providing input for budget planning, delivering assignments with quality and within timelines, overseeing contingent workers and/or vendors, and leading/co-leading clinical programming for studies or regulatory submissions. You will also be involved in developing, reviewing, documenting, and validating generic SAS macros, as well as initiating and leading new processes and methodologies to improve operational efficiency. To qualify for this role, you should have a Bachelor's Degree, Master's Degree, or PhD in Science, Statistics, Information Technology, or a related field, along with relevant work experience. Specifically, a Bachelor's Degree plus 3 years or a Master's Degree plus 2 years of experience is preferred. Additionally, experience in SDTM and ADaM, familiarity with CDISC Guidelines, and a commitment to Teva's Equal Employment Opportunity principles are essential. If you are passionate about making a difference in the pharmaceutical industry and eager to contribute your clinical programming expertise to a leading global manufacturer of generic medicines, we encourage you to apply for the R&D Programmer III position at Teva Pharmaceuticals today.,

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