R&D Programmer – Clinical Programming Lead Manager
Company: Teva Pharmaceuticals
Location: Bangalore, Karnataka, India (560064)
Job Type: Full-Time
Category: Clinical Data Management / Clinical Programming / R&D
Experience Required: 8+ years
Company Overview
Teva Pharmaceuticals is a global leader in generic medicines and specialty pharmaceuticals, committed to making health more affordable and accessible. With operations in nearly 60 countries, Teva reaches over 200 million patients worldwide daily through medicines included in the World Health Organization’s Essential Medicines List. Teva fosters a diverse, inclusive work environment and promotes innovation in pharmaceutical research and development.
Job Summary
Teva Pharmaceuticals is seeking an experienced Clinical Programming Lead Manager to oversee and execute clinical programming and data management activities across multiple trials. This role ensures accurate, timely, and compliant delivery of clinical data, working closely with CROs, third-party vendors, and internal teams to maintain data integrity and adherence to CDISC standards.
The ideal candidate combines technical expertise in clinical programming (SAS/SQL), SDTM mapping, and CDISC compliance with leadership experience to support data operations, drive process improvements, and mentor team members.
Key Responsibilities
Clinical Programming & Data Management
Lead programming and data operations for clinical trials, ensuring milestone deliverables are met.
Manage data definition and coordinate with CROs/third-party vendors to ensure data is received in Teva’s standard formats.
Generate Database Transfer Specifications (DTS) and process study-related datasets efficiently.
Maintain SDTM/CDISC standards across studies and integrate external data sources such as laboratory and questionnaire data.
Support mapping SDTM domains and manage metadata within Teva’s SCE/CDR environment.
Technical Expertise
Proficient in SAS programming and SQL for clinical trial data management.
Strong knowledge of CDISC standards, including SDTM mapping and SDTM IG compliance.
Experience with MaxisIT SCE and CDR platforms is advantageous.
Ensure all data management activities meet quality, regulatory, and sponsor requirements.
Leadership & Process Improvement
Provide leadership and guidance for departmental tasks, promoting best practices in clinical data operations.
Drive continuous improvement initiatives to enhance data quality, standardization, and workflow efficiency.
Mentor junior programming staff and support team development.
Work Allocation
~75% focus on SCE tasks (standards management, loading questionnaires, metadata updates)
~25% focus on SDTM domain mapping and integration
Education & Experience Requirements
Bachelor’s degree + 10 years or Master’s degree + 8 years of relevant experience in pharmaceutical or clinical research programming
Degrees in Science, Statistics, Information Technology, or related field
Minimum 8+ years of SAS programming experience
Strong understanding of Clinical Data, SDTM IG, Pinnacle 21, and CDISC standards
Skills & Competencies
Expertise in clinical trial data management and programming
Advanced proficiency in SAS and SQL for data extraction, transformation, and validation
Knowledge of SDTM, ADaM, CDISC standards, and clinical trial database structure
Strong analytical, problem-solving, and organizational skills
Ability to work independently and manage multiple projects simultaneously
Excellent communication, collaboration, and team leadership skills
Familiarity with CRO/vendor management and study startup processes
Why Join Teva
Work with a global pharmaceutical leader impacting millions of patients worldwide
Gain exposure to complex clinical trials and advanced data operations
Contribute to innovative R&D initiatives in a collaborative, inclusive environment
Opportunities to lead, mentor, and grow within a multinational organization
Be part of a mission to improve global health access and affordability
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