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الوصف الوظيفي

Who we are

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.




The opportunity

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


The Senior Manager leads and manages completed projects that involve global tasks, cross functional teams, or outsourcing resources. The role may require providing inputs to design and analysis, and reporting 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.




How you’ll spend your day
  • Primarily works at the product / program level 
  • Possible to have direct reports; Likely to oversee contingent workers and/or vendors; likely to provide training to others; Analyzes needs to manage resources
  • Provides input for Budget Planning
  • Manages and Delivers assignments with quality and within timelines
  • 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.
  • 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.  
  • Responsible for the standardization of GSD 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.
  • Leads global projects with cross-functional involvement; demonstrate project management and leadership capabilities.


Your experience and qualifications
  • Bachelor’s Degree/Master’s Degree/PhD in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
  • Bachelor’s Degree/Master’s Degree/PhD in Science, Statistics, Information Technology or equivalent combination of education and related work experience.
  • Expert level of programming skills and problem resolution in SAS. Provide programming and documentation support for SAS system development


Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.






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