Job Description

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 Senior Clinical Programmer is responsible to provide high level skills of clinical programming support of clinical projects and regulatory submissions. The Senior Clinical Programmer is playing a lead role generating and validating analysis datasets, tables, listings and figures. The Senior Clinical Programmer participates in the development of global data standards, SDTM, ADaM and Teva\'s database structure. The Senior Clinical Programmer is responsible for providing professional expertise and leadership through leading departmental tasks and taking initiatives in improving clinical programming processes with focus on SAS Programming.

How you\'ll spend your day

Primarily work on the departmental processes like managing databases in Oracle which support SDTM standards infrastructure.

• Ensure timely, efficient and high-quality deliverables.
• Need a thorough understanding of ETL processes to support operational data processing for Clinical databases
• Participate in creating and managing tables, indexes, db links and privileges.
• Create stored packages, procedure, and function to implement the data extraction and transformation logic.
• Lead implementation of business applications, using SDLC methodology.
• Conduct technical design review meetings with system analysts and QA team and seek approval for development.
• Perform and document unit testing.
• Work with Vendors to participate in Clinical study start-up activities using CDMS and other Clinical Vendors like Lab or EC
• Experience in authoring DTS
• Thorough understanding of Clinical trial process

Your experience and qualifications

• Bachelor\'s degree or higher in the areas of Science, Statistics, Information Technology or equivalent combination of education and related work experience.
• 4+ years of professional experience in a pharmaceutical or clinical research setting as a programmer.
• 5-7 years of Oracle experience
• Experience in SDTM acquainted with CDISC Guidelines
• 4+ years of SAS experience

Enjoy a more rewarding choice

Make a difference with Teva Pharmaceuticals

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:

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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.

Teva Pharmaceuticals