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R&D Programmer Iii

3+ years
Not Disclosed
10 March 21, 2025
Job Description
Job Type: Full Time Education: B.Com/ BBA/ MBA/ M.Com/ B.Sc/ M.Sc/ B.Tech/ M.Tech/ 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, helping millions worldwide achieve better health. With operations in nearly 60 countries and a diverse workforce, Teva manufactures many products on the World Health Organization's Essential Medicines List. Every day, 200 million people take one of our medicines, and we are committed to finding new ways to make an impact and bring positive change.

The Opportunity:

We are seeking a Senior Clinical Programmer to provide high-level clinical programming support for clinical projects and regulatory submissions. The Senior Clinical Programmer plays a lead role in generating and validating analysis datasets, tables, listings, and figures. This role involves contributing to the development of global data standards, including SDTM, ADaM, and Teva’s database structure. The Senior Clinical Programmer is also responsible for leading departmental tasks and improving clinical programming processes, with a strong focus on SAS programming.

How You’ll Spend Your Day:

  • Project-Level Work:

    • Primarily works at the project level and provides input for budget planning.

    • Delivers assignments with quality and within defined timelines.

  • Leadership & Training:

    • May oversee contingent workers and/or vendors and provide training as needed.

    • Leads/co-leads clinical programming for studies or regulatory submissions.

  • SAS Programming & Validation:

    • Develops, reviews, documents, and validates generic SAS macros.

    • Ensures compliance with CDISC guidelines and requirements.

  • Process Improvement:

    • Initiates and leads new processes, methodologies, and operational ideas to improve effectiveness and efficiency.

    • Supervises and supports outsourcing activities when required.

Your Experience and Qualifications:

  • Education:

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

  • Experience:

    • Bachelor’s Degree +3 years or Master’s Degree +2 years of related work experience.

    • Strong knowledge of SDTM and ADaM, with familiarity with CDISC Guidelines and requirements.

Teva’s Equal Employment Opportunity Commitment:

Teva Pharmaceuticals is committed to providing equal employment opportunities regardless of age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national origin, or any other legally protected status. We promote a diverse and inclusive workplace, ensuring that all applicants receive a fair and accessible recruitment process.