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Sr Mgr Statistical Programming

3+ years
Not Disclosed
10 March 21, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/PhD/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

Sr Manager, Statistical Programming - 60153

Company: Teva Pharmaceuticals
Location: Bangalore, India, 560064
Date: March 18, 2025

Who We Are:
Teva Pharmaceuticals is committed to making healthcare more affordable and accessible in over 60 countries, improving the lives of millions worldwide. As the world’s leading manufacturer of generic medicines and a producer of many products on the World Health Organization's Essential Medicines List, Teva impacts at least 200 million people daily.

The Opportunity:
The Senior Manager, Clinical Programming, is responsible for managing the timely and accurate execution of programming components in clinical trials. The role involves leading global projects, managing cross-functional teams, and overseeing outsourced resources. It includes providing input on trial design, analysis, and reporting, including programming rules and table/listing/graph (T/L/G) mock-ups. The position also supports safety claims for new drugs and provides publication support for marketed drugs.

How You’ll Spend Your Day:

  • Work primarily at the product/program level.

  • Potentially oversee contingent workers/vendors and provide training to others.

  • Analyze needs and manage resources effectively.

  • Provide input for budget planning.

  • Ensure assignment completion with quality and within timelines.

  • Offer strong programming support for CDISC-based e-submissions.

  • Develop, review, and validate generic macros.

  • Develop, debug, and enhance SAS programs to support quality control of safety and efficacy derived datasets.

  • Implement programming standards and comply with regulatory requirements across project teams.

  • Standardize GSD deliverables across study projects.

  • Define programming rules and standardization across therapeutic areas/indications.

  • Lead global projects with cross-functional involvement and demonstrate 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.

  • Technical Skills:

    • Expert-level programming skills and problem-solving abilities in SAS.

    • Ability to provide programming and documentation support for SAS system development.

    • Experience in managing programming standards and ensuring regulatory compliance.

Teva’s Equal Employment Opportunity Commitment:
Teva Pharmaceuticals is dedicated to providing equal employment opportunities regardless of age, race, creed, religion, sex, disability, medical condition, sexual orientation, gender identity, national origin, or any other legally recognized status. We are committed to fostering a diverse and inclusive workplace.