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Teva Pharmaceuticals
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Sr Mgr Statistical Programming

Sr Mgr Statistical Programming

Teva Pharmaceuticals

10 - 14 years

0 Lacs

karnataka

Posted:1 week ago| Platform: Shine logo

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Skills Required

statistical programming clinical trials sas data presentation regulatory requirements project management leadership cdisc

Work Mode

On-site

Job Type

Full Time

Job Description

Role Overview: You will be working as a Senior Manager, Statistical Programming, providing comprehensive programming leadership for programming deliverables within a product/program. Your role will involve managing the timely and accurate execution of programming components of clinical trials to support the development, regulatory approval, and market acceptance of Teva Products. You will also lead and manage projects that involve global tasks, cross-functional teams, or outsourcing resources. Key Responsibilities: - Primarily work at the product/program level - Manage and deliver assignments with quality and within timelines, providing input for budget planning - Independently develop, validate, and maintain complex programs and utilities in accordance with predefined specifications and standards - Provide strong programming support to CDISC based e-submission - Review key planning documents to ensure alignment with project objectives, contribute to the development of data presentation plan (DPP), programming specifications, regulatory reviewers guide documents, and ensure clarity and completeness of programming requirements - Implement programming standards and comply with regulatory requirements among project team members and across all projects - Responsible for the standardization of GSD deliverables across study projects within an indication/therapeutic area - Contribute to the overall definition of programming rules and standardization across therapeutic areas and/or indication - Identify, support process and technology improvement initiatives, communicate proactively and effectively around issues and risks, and contribute to remediation strategies - Lead global projects with cross-functional involvement and demonstrate project management and leadership capabilities - Contribute to departmental policies, standards, and best practices Qualifications Required: - Bachelors Degree/Masters Degree in Science, Statistics, Information Technology, or equivalent combination of education and related work experience - Bachelors + 12 years, Masters + 10 years in a pharmaceutical or clinical research setting as a programmer - Expert level of programming skills and problem resolution in SAS or other Statistical programming software - Provide programming and documentation support for SAS (or other Statistical software) system development Additional Company Details: Teva is on a mission to make good health more affordable and accessible, helping millions around the world enjoy healthier lives. They are the world's leading manufacturer of generic medicines and producer of products on the World Health Organization's Essential Medicines List. Teva aims to continue making a difference and is always looking for new ways to impact positively. (Note: The Equal Employment Opportunity Commitment section has been omitted as it does not contain specific details relevant to the job description.),

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Teva Pharmaceuticals

Pharmaceutical Manufacturing

Tel-Aviv Petach Tikva

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Sr Mgr Statistical Programming