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2.0 - 6.0 years
0 Lacs
karnataka
On-site
Role Overview: As an R&D Programmer III at Teva Pharmaceuticals, you will play a crucial role in providing high-level clinical programming support for clinical projects and regulatory submissions. Your responsibilities will include generating and validating analysis datasets, tables, listings, and figures. You will also contribute to the development of global data standards, such as SDTM, ADaM, and Teva's database structure. Additionally, you will lead departmental tasks, drive initiatives to enhance clinical programming processes, and focus on SAS Programming. Key Responsibilities: - Work at the project level and provide input for budget planning - Deliver assignments with quality and withi...
Posted 1 month ago
2.0 - 6.0 years
0 Lacs
karnataka
On-site
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, overseein...
Posted 3 months ago
15.0 - 19.0 years
0 Lacs
karnataka
On-site
As the Manager of Data Management at eClinical Solutions, you will be responsible for providing operational leadership in overseeing end-to-end data management services for designated projects and studies in modern clinical data management. Your role will involve collaborating closely with clients and vendors to ensure timely delivery of high-quality outputs within budgetary constraints. You will strategically integrate advanced technologies and data science techniques to enhance the efficiency and quality of clinical trials within our organization, aiming to improve operational effectiveness and scientific rigor in data management practices. Your key tasks and responsibilities will include:...
Posted 3 months ago
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