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R&D Programmer Iv

0-2 years
Not Disclosed
10 Feb. 12, 2025
Job Description
Job Type: Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences 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

Job Title: R&D Programmer IV
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job ID: 60622
Date: February 3, 2025

About Teva Pharmaceuticals:

Teva Pharmaceuticals is the world’s leading manufacturer of generic medicines, helping millions of people around the world enjoy healthier lives. With a mission to make good health more affordable and accessible, Teva is a key player in the global pharmaceutical industry. The company is committed to innovation and improving global healthcare, and today, more than 200 million people around the world rely on Teva’s medicines every single day.

The Opportunity:

As an R&D Programmer IV, you will manage the timely and accurate execution of programming components for clinical trials. You will be leading and managing completed projects that involve global tasks, cross-functional teams, or outsourcing resources. Your responsibilities will include providing programming support for regulatory submissions, designing programming rules, and reporting clinical trial results. In addition, you will provide support for safety claims for new drugs and extensions for marketed drugs.

Key Responsibilities:

  • Leadership & Management: Lead global projects, oversee project management, and provide guidance to outsourcing programmers and CROs.
  • Programming Support: Provide strong programming support for CDISC-based e-submissions and validate generic macros. Develop and enhance SAS programs for safety or efficacy-derived datasets.
  • Collaboration: Work closely with the clinical team, data management, statisticians, and project physicians. Participate in project meetings and act as the main programming contact for clinical teams.
  • Data Accuracy: Ensure the accuracy and validity of study databases (SDTM/ADaM), data displays, and programming deliverables for regulatory submissions (NDA/MAA/IND/PSUR).
  • Methodology & Process: Extend or develop new clinical programming methods to solve complex problems and improve programming processes.
  • Training & Mentorship: Mentor and train selected associates within the Biometrics group, especially in SAS programming techniques.

Qualifications & Experience:

  • Education: Bachelor’s or higher degree in Science, Statistics, Information Technology, or related field.
  • Experience: More than 7 years of professional experience in pharmaceutical or clinical research.
  • Skills: Advanced SAS knowledge, including SAS Base, SAS Report Writing, and SAS Macros/Functions.

Teva’s Equal Employment Opportunity Commitment:

Teva Pharmaceuticals is committed to providing equal employment opportunities regardless of age, race, religion, sex, disability, sexual orientation, gender identity, or any other protected status. The company fosters a diverse and inclusive work environment, ensuring that all candidates receive equal consideration and accommodations during the recruitment process.

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For more information, visit Teva Pharmaceuticals Careers.