R&D Programmer Iii

3+ years

Not Disclosed

Bangalore

10 April 18, 2025

Job Description

Job Type: Full Time Education: PhD/B.Sc./M.Sc./B.Pharm/M.Pharm/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 III

Date: April 12, 2025
Location: Bangalore, India, 560064
Company: Teva Pharmaceuticals
Job ID: 60149

Who we are:
Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

The opportunity:
The Senior Clinical Programmer is responsible for providing high-level clinical programming support to clinical projects and regulatory submissions. This role involves taking a lead position in generating and validating analysis datasets, tables, listings, and figures. The Senior Clinical Programmer actively participates in the development of global data standards, SDTM, ADaM, and Teva’s database structures, offering professional expertise and leadership through departmental initiatives aimed at improving clinical programming processes, with a focus on SAS programming.

How you’ll spend your day:

Primarily work at the project level.
Provide input for budget planning.
Deliver assignments with quality and within timelines.
Oversee contingent workers and/or vendors; provide training to others as needed.
Lead/co-lead clinical programming for a study or regulatory submission.
Develop, review, document, and perform validation of generic SAS macros.
Initiate and lead new processes, methodologies, and operational improvements; challenge existing processes to enhance effectiveness and efficiency.
Supervise and support outsourcing activities.

Your experience and qualifications:

Bachelor’s Degree, Master’s Degree, or PhD in Science, Statistics, Information Technology, or an equivalent combination of education and related work experience.
Bachelor’s Degree + 3 years, or Master’s Degree + 2 years of experience in Science, Statistics, Information Technology, or related fields.
Experience with SDTM and ADaM, well-versed in CDISC Guidelines and requirements.

Teva’s Equal Employment Opportunity Commitment:
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity is provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin, or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used solely to provide an accessible candidate experience.

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R&D Programmer Iii

Job Description

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