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R&D Programmer Iii

3-4 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 III
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job ID: 60149
Date: January 15, 2025

About Teva Pharmaceuticals:

Teva Pharmaceuticals is dedicated to improving lives globally by making healthcare more affordable and accessible. With a mission to help millions of people lead healthier lives, Teva manufactures generic medicines and is a major contributor to the World Health Organization’s Essential Medicines List. Over 200 million people take Teva’s medicines every day. The company is constantly seeking innovative ways to make a difference in healthcare.

The Opportunity:

The R&D Programmer III is responsible for providing high-level clinical programming support for clinical projects and regulatory submissions. The role involves generating and validating analysis datasets, tables, listings, and figures, while participating in the development of global data standards (such as SDTM, ADaM). This position also focuses on SAS programming, providing leadership in clinical programming processes, and overseeing departmental tasks and outsourcing activities.

Key Responsibilities:

  • Clinical Programming: Lead clinical programming tasks for studies or regulatory submissions, including generating analysis datasets, tables, listings, and figures.
  • Development of Standards: Participate in the development of global data standards, including SDTM and ADaM, and help design Teva’s database structure.
  • Leadership and Training: Lead clinical programming for projects, providing mentorship and training to team members and overseeing contingent workers or vendors.
  • Process Improvement: Lead the development of new processes and methodologies to enhance the effectiveness and efficiency of services provided.
  • Outsourcing Support: Supervise and support outsourcing activities to ensure timely and accurate completion of tasks.
  • SAS Programming: Develop, review, document, and validate SAS macros for clinical data analysis and reporting.

Qualifications & Experience:

  • Education: Bachelor's degree or Master's degree/PhD in Science, Statistics, Information Technology, or a related field. A minimum of 2-3 years of relevant work experience with a Master's or 3+ years with a Bachelor's degree.
  • Experience: Proficient in SDTM and ADaM, with knowledge of CDISC guidelines and requirements.
  • Skills: Strong expertise in SAS programming for clinical data analysis, as well as experience in leading clinical programming teams.

Teva’s Equal Employment Opportunity Commitment:

Teva Pharmaceuticals is committed to providing equal employment opportunities without discrimination based on age, race, gender, disability, or any other legally protected status. The company fosters a diverse and inclusive workplace and ensures accommodations are made for candidates throughout the recruitment process.

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For more details, visit Teva Pharmaceuticals Careers.