Senior Manager – Statistical Programming (Clinical Trials)
Company: Teva Pharmaceuticals
Location: Bangalore, India
Employment Type: Full-Time
Function: Biostatistics & Statistical Programming
Industry: Pharmaceuticals & Life Sciences
Experience Required: 10–12+ Years
Job ID: 64313
Posting Date: December 9, 2025
About Teva Pharmaceuticals
Teva Pharmaceuticals is a global leader in generic and specialty medicines, operating across nearly 60 countries and supporting the health of more than 200 million patients daily. As a major contributor to medicines on the WHO Essential Medicines List, Teva is driven by science, quality, and a mission to make healthcare more affordable and accessible worldwide.
Role Overview
The Senior Manager – Statistical Programming provides strategic and operational leadership for statistical programming deliverables across clinical development programs. This role is critical to the successful execution, analysis, and regulatory submission of clinical trials supporting Teva’s global product portfolio.
The position involves managing complex global projects, leading internal teams and external vendors, supporting regulatory submissions, and driving standardization, innovation, and process excellence within statistical programming.
Key Responsibilities
Programming Leadership & Project Oversight
Lead statistical programming activities at the product and program level across multiple clinical studies
Manage global, cross-functional projects involving internal teams, vendors, and outsourced partners
Provide mentoring, training, and technical guidance to junior programmers and contingent resources
Plan and allocate resources effectively, contributing to budget planning and forecasting
Statistical Programming & Regulatory Support
Independently develop, validate, and maintain complex statistical programs and utilities in accordance with internal standards and regulatory requirements
Provide expert programming support for CDISC-based eCTD submissions (SDTM, ADaM, TLGs)
Develop, review, validate, and maintain SAS macros or equivalent statistical programming tools
Support programming and quality control of safety and efficacy datasets
Clinical Trial Data & Documentation
Review key clinical documents including protocols, statistical analysis plans (SAPs), and regulatory guidance to ensure alignment with programming deliverables
Contribute to the development of:
Data Presentation Plans (DPPs)
Programming specifications (SDTM and ADaM)
Regulatory Reviewer’s Guides
Ensure clarity, completeness, and robustness of programming assumptions and outputs
Standards, Compliance & Process Improvement
Implement and enforce programming standards across projects and therapeutic areas
Drive standardization of global statistical deliverables within assigned indications
Contribute to the definition of programming rules, visualization standards, and best practices
Identify risks, proactively communicate issues, and support remediation strategies
Lead and support process optimization, technology enhancements, and change management initiatives
Departmental & Strategic Contributions
Support departmental policy development, SOPs, and best practices
Provide regular project updates to senior leadership on timelines, quality, and resource utilization
Required Experience & Qualifications
Education:
Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, Information Technology, Life Sciences, or a related discipline
Experience:
Bachelor’s degree + 12 years or Master’s degree + 10 years of experience as a statistical programmer in the pharmaceutical, biotech, or clinical research (CRO) industry
Extensive hands-on experience with clinical trial programming and regulatory submissions
Technical Expertise:
Expert-level proficiency in SAS or equivalent statistical programming software
Strong experience supporting CDISC standards, regulatory documentation, and submission-ready datasets
Proven ability to develop, debug, validate, and document complex statistical programs
Core Competencies:
Strong leadership, project management, and mentoring skills
Excellent analytical, problem-solving, and communication abilities
Ability to manage multiple priorities in a fast-paced, global environment
Reporting Line
Reports to: Director – Statistical Programming
Why Join Teva
Lead high-impact global clinical development programs
Work on regulatory submissions supporting medicines used by millions worldwide
Influence programming strategy, standards, and innovation across therapeutic areas
Collaborate with global experts in biostatistics, clinical development, and regulatory affairs
Long-term career growth in a science-driven, patient-focused organization
Equal Employment Opportunity
Teva Pharmaceuticals is an Equal Opportunity Employer committed to fostering a diverse and inclusive workplace. Employment decisions are made without regard to age, race, religion, gender, disability, pregnancy, sexual orientation, gender identity or expression, national origin, or any other legally protected status. Reasonable accommodations are available throughout the recruitment process upon request.
SEO Keywords for Visibility
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