R&D Programmer

Date: Dec 17, 2025

Location:

Bangalore, India, 560064

Company: Teva Pharmaceuticals

Job Id: 62014

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 Lead Manager is responsible for managing timely and accurate execution of all start-up activities and milestone deliverables for all assigned clinical trial projects. Clinical Programming lead manager is responsible for data definition by working with CRO and Third-Party Vendors (TPV) to ensure receipt of data in Teva data standard format, generating the database transfer specification (DTS), receiving and processing study related data. This position is also responsible for providing professional expertise and leadership through leading departmental tasks and taking initiatives in improving data management processes with focus on Data Operations activities.

How you’ll spend your day

Proficient in SQL and SAS programming.
Strong knowledge of SDTM mapping and CDISC standards.
Experience with MaxisIT SCE and CDR is a plus.
Will support integration of external data sources (e.g., labs and questionnaires) into the SCE/CDR environment.
Wil manage and maintain SDTM CDISC standards across studies.
Work allocation:

75% on SCE tasks (managing standards, loading questionnaires and metadata).
25% on mapping SDTM domains.

Your experience and qualifications

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

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: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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.