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R&D Programmer Iii

3+ years
Not Disclosed
10 March 26, 2025
Job Description
Job Type: Full Time Education: B.Tech/PhD/B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

R&D Programmer III
Date: March 14, 2025
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job ID: 60149


Who We Are:
Teva Pharmaceuticals is a global leader in generic medicines and a proud producer of numerous products on the World Health Organization’s Essential Medicines List. With operations in nearly 60 countries and a diverse workforce, we serve millions worldwide by making healthcare more affordable and accessible. Today, at least 200 million people globally take one of our medicines daily, and we’re continuously striving to extend our positive impact by innovating and bringing in new talent.


The Opportunity:
As a Senior Clinical Programmer in R&D Programming, you will provide advanced clinical programming support for clinical projects and regulatory submissions. You will play a leading role in generating and validating analysis datasets, tables, listings, and figures. You will also contribute to the development of global data standards, SDTM, ADaM, and Teva’s database structure while taking initiatives to enhance clinical programming processes, with a strong focus on SAS Programming.


How You’ll Spend Your Day:

  • Project-Level Responsibility: Primarily work at the project level, ensuring quality and on-time delivery.

  • Budget Input: Provide input for budget planning and resource management.

  • Vendor Management: Oversee contingent workers and vendors, providing training when necessary.

  • Clinical Programming Leadership: Lead or co-lead clinical programming for a study or regulatory submission.

  • SAS Macro Development: Develop, review, document, and validate generic SAS macros.

  • Process Improvement: Initiate and lead new processes, methodologies, and operational ideas to enhance effectiveness and efficiency.

  • Outsourcing Supervision: Supervise and support outsourcing activities to ensure quality outcomes.


Your Experience and Qualifications:

  • Education:

    • Bachelor’s Degree, Master’s Degree, or PhD in Science, Statistics, Information Technology, or a related field.

  • Experience:

    • Bachelor’s Degree with 3+ years of experience, or

    • Master’s Degree with 2+ years of experience in clinical programming, data analysis, or a similar role.

  • Technical Knowledge:

    • Experience in SDTM and ADaM, with knowledge of CDISC Guidelines and Requirements.

    • Proficiency in SAS Programming with a strong focus on clinical data analysis and reporting.


Teva’s Equal Employment Opportunity Commitment:
Teva Pharmaceuticals is committed to equal opportunity in employment. We ensure that all qualified applicants are considered 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 protected status.

If you are contacted for a job opportunity, please inform us of any accommodations needed to facilitate an inclusive and accessible candidate experience.