Sr Manager, Statistical Programming
Date: March 14, 2025
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job ID: 60152
Who We Are:
Teva Pharmaceuticals is a global leader in generic medicines and a key contributor to the World Health Organization’s Essential Medicines List. Operating across nearly 60 countries with a diverse workforce, we strive to make healthcare affordable and accessible, helping millions worldwide enjoy healthier lives. With 200 million people using our medicines daily, we are constantly seeking innovative ways to expand our impact and welcome new talent to contribute to this mission.
The Opportunity:
The Senior Manager, Clinical Programming is responsible for managing the timely and accurate execution of programming components for clinical trials. This role involves leading global projects, managing cross-functional teams and vendors, and contributing to the design, analysis, and reporting of clinical trials. The Senior Manager also ensures compliance with programming standards and regulatory requirements and supports safety claims for new and marketed drugs.
How You’ll Spend Your Day:
Product/Program Level Oversight: Manages programming components for clinical trials at the product/program level.
Team and Vendor Management: May have direct reports, oversee contingent workers and/or vendors, and provide training as needed.
Resource and Budget Planning: Analyzes needs to manage resources and provides input for budget planning.
Timely and Quality Deliverables: Ensures assignments are completed on time and with high quality.
e-Submission and CDISC Support: Provides strong programming support for CDISC-based e-submissions and validates generic macros.
SAS Programming and Debugging: Develops, reviews, and enhances SAS programs to support quality control of safety and efficacy datasets.
Regulatory Compliance: Implements programming standards, ensures compliance with regulatory requirements, and communicates project status and resource needs to management.
Standardization Across Projects: Responsible for standardizing GSD deliverables across study projects within an indication or therapeutic area.
Cross-Functional Leadership: Leads global projects with cross-functional involvement, demonstrating strong project management and leadership capabilities.
Your Experience and Qualifications:
Education:
Bachelor’s, Master’s, or PhD in Science, Statistics, Information Technology, or a related field, or an equivalent combination of education and related work experience.
Skills:
Expert-level programming skills and problem resolution in SAS.
Ability to provide programming and documentation support for SAS system development.
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.
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