R&d Programmer Iv jobs at Teva in India, Bengaluru

• Primarily work at the project level
• Provides input for budget planning
• Delivers assignments with quality and within timelines
• May oversee contingent workers and/or vendors; may provide training to others as needed
• Leads/co-leads clinical programming for a study or for a study or for a regulatory submission
• Develops, reviews, documents and performs validation of generic SAS macros
• Initiates and leads new processes, new methodologies and operational ideas; challenge existing ones to improve the effectiveness and efficiency of services provided
• Supervises and supports outsourcing activities

• Bachelor’s Degree/master’s degree/PhD in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
• Bachelor’s Degree +3 years or master’s degree +2 years in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
• Experience in SDTM and ADaM acquainted with CDISC Guidelines and requirements.

• Manages multiple projects
• Likely to oversee contingent workers and/or vendors; Likely to provide training/Mentoring to others
• Ensures accurate set-up of data transfer processing
• Delivers assignments with quality and within timelines
• Provides strong programming support to CDISC based e-submission. Develops, debugs, and enhances SAS/ SQL programs to support to support study data batch processing and oversight listings
• Responsible to define case report forms (CRFs) and external (non CRF) data specifications in accordance with CDISC guideline and Teva standards
• Responsible to define data flow and additional startup activities related to study initiation
• Responsible to perform, supervise and manage day-to-day activities associated with receipt of clinical (CRF and non CRF) and operational (when relevant) data in accordance with study timelines
• Responsible to perform data handling activities/unblinding activities on an ongoing basis to ensure accuracy, reliability, integrity, consistency and completeness of the data prior to database lock and providing the final data to clinical programming and statistics after database lock

• Bachelor’s + 10 years or Master’s + 8 years of professional experience in a pharmaceutical or clinical research setting as a programmer
• Bachelor’s Degree/ Master’s Degree/ PhD in Science, Statistics, Information Technology or equivalent combination of education and related work experience
• Thorough understanding of Clinical data, SDTM IG and Pinnacle 21
• 8+ years of SAS Programming experience

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• Manages multiple projects
• Likely to oversee contingent workers and/or vendors; Likely to provide training/ Mentoring to others
• Ensures accurate set-up of data transfer processing
• Delivers assignments with quality and within timelines
• Provides strong programming support to CDISC based e-submission. Develops, debugs, and enhances SAS/ SQL programs to support to support study data batch processing and oversight listings
• Responsible to define case report forms (CRFs) and external (non CRF) data specifications in accordance with CDISC guideline and Teva standards.
• Responsible to define data flow and additional startup activities related to study initiation
• Responsible to perform, supervise and manage day-to-day activities associated with receipt of clinical (CRF and non CRF) and operational (when relevant) data in accordance with study timelines
• Responsible to perform data handling activities/unblinding activities on an ongoing basis to ensure accuracy, reliability, integrity, consistency and completeness of the data prior to database lock and providing the final data to clinical programming and statistics after database lock

• Bachelor’s + 10 years or Master’s + 8 years of professional experience in a pharmaceutical or clinical research setting as a programmer
• Bachelor’s Degree/ Master’s Degree/ PhD in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
• Thorough understanding of Clinical data, SDTM IG and Pinnacle 21
• 8+ years of SAS Programming experience

The Clinical Programming Manager is responsible to manage the timely and accurate execution of programming components of clinical trials. The Manager leads and manages completed projects, that involved global tasks or cross functional teams or outsourcing resources. The role may require providing inputs 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.

• Being able to accomplish all the major duties of Senior SAS Programmer
• Leading global projects with cross functional involvement and required project management and leadership capabilities
• Supervise or mentor CROs or outsourcing programmers
• Providing 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
• Have good knowledge of understanding the statistical models in efficacy data analysis.
• Implement programming standards and comply with regulatory requirements among project team members and across all projects; communicate to management on project status and resource issues
• Core member of clinical team and main programming contact with the DM team, statistician and project physician.
• Responsible for the standardization of Biometrics deliverables across study projects within an indication/therapeutic area.
• Responsible for the overall definition of programming rules and standardization across therapeutic areas and/or indication.
• Coordinating Clinical Programming resources, priorities and timelines with the clinical team
• Participation in project team meetings.
• Extending existing or developing new clinical programming methods to solve complex problems
• Ensuring the accuracy and validity of data displays.
• Ensuring the accuracy and validity of the study database (SDTM) and/or analysis database (ADaM), as applicable.
• Primary responsible for all programming deliverables for NDA/MAA/IND/PSUR.
• Work closely with Statistics group for the production of tables, listings and graphs as applicable.
• Mentor and train selected associates within the Biometrics group for SAS programming.
• Miscellaneous activities directed by management.

• Bachelor’s or higher degree in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
• More than 7 years of professional experience in pharmaceutical or clinical research
• Excellent SAS knowledge of the following SAS modules/procedures: Base SAS; SAS report writing, SAS macros/functions.

• Primarily work at the project level
• Provides input for budget planning
• Delivers assignments with quality and within timelines
• May oversee contingent workers and/or vendors; may provide training to others as needed
• Leads/co-leads clinical programming for a study or for a study or for a regulatory submission
• Develops, reviews, documents and performs validation of generic SAS macros
• Initiates and leads new processes, new methodologies and operational ideas; challenge existing ones to improve the effectiveness and efficiency of services provided
• Supervises and supports outsourcing activities

• Bachelor’s Degree/master’s degree/PhD in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
• Bachelor’s Degree +3 years or master’s degree +2 years in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
• Experience in SDTM and ADaM acquainted with CDISC Guidelines and requirements.

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.