Instagram
youtube
Facebook

R&D Programmer Iv

5+ 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

R&D Programmer IV - Teva Pharmaceuticals - 61013

Date: March 11, 2025
Location: Bangalore, India, 560064

Who we are:
Teva Pharmaceuticals is dedicated to making good health more affordable and accessible across nearly 60 countries, impacting over 200 million people daily. As the world's leading manufacturer of generic medicines and a producer of many WHO-listed essential medicines, Teva continues to innovate and make a difference.

The opportunity:
The Clinical Programming Manager is responsible for managing the timely and accurate execution of programming components of clinical trials. This role involves leading global tasks, managing cross-functional teams, and providing support for the development and validation of programming models for clinical trial data.

How you’ll spend your day:

  • Budget Planning: Provides input for budget planning and resource allocation.

  • Vendor and Team Management: Oversees contingent workers and/or vendors, and may provide training to others.

  • Project-Level Work: Delivers assignments with quality and within specified timelines.

  • Strategic Contribution: Contributes to project strategy under moderate supervision.

  • Programming Support: Provides strong programming support for CDISC-based e-submissions, including development, review, and validation of generic macros.

  • SAS Programming: Develops, debugs, and enhances SAS programs to support quality control of safety and efficacy datasets.

  • Statistical Analysis Knowledge: Applies good knowledge and understanding of statistical models in efficacy data analysis.

  • Standardization: Ensures standardization of Clinical Programming deliverables within a project.

  • Problem Solving: Extends existing or develops new clinical programming methods to solve complex problems.

Your experience and qualifications:

Education:

  • Bachelor’s Degree / Master’s Degree / PhD in Science, Statistics, Information Technology, or a related field.

  • Equivalent combination of education and related work experience is acceptable.

Experience:

  • Bachelor’s + 5 years or Master’s + 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer.

  • Experience in SDTM and ADaM with familiarity with CDISC Guidelines and requirements.

Teva’s Equal Employment Opportunity Commitment:
Teva Pharmaceuticals is committed to equal opportunity in employment regardless of legally protected statuses. We are dedicated to fostering a diverse and inclusive workplace for all.