Senior Statistical Programmer

Work Your Magic with us! 

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That`s why we are always looking for curious minds that see themselves imagining the unimageable with us.

Your role:  

Under the supervision of a Project Statistical Programmer, you will function as Statistical Programmer for one or more clinical trials and/or other global project sub tasks, across one or more clinical development programs. Specifically, you will be responsible for the statistical programming deliverables according to defined project timelines and quality expectations to achieve project goals. You will coordinate basic statistical programming aspects of trials or other project subtasks and can lead standard subtasks. Additionally, you can independently develop, validate, troubleshoot, and maintain complex programs in accordance with defined specifications and standards. In this role, you will provide expert statistical programming advice, guidance, and training to junior trial team members.   In addition, you may contribute to departmental innovation and process improvement projects. 

Statistical Programming activities:

•Programming skills: R programming and SAS (at least SAS/BASE, SAS/STAT, SAS/MACRO,SAS/GRAPH, SQL)

•Totally familiar with CDISC ADaM (including specifications, Define.xml and ADRG) and its concepts

•Ability to provide solutions for complex programming issues (including creation of complex macros presenting alternatives and identifying the best solution

Who you are:

• BSc or MSc in Computer Science, Mathematics, Statistics, or related health science
• 4-7 years of experience in the pharmaceutical industry including support of regulatory filings. Experience in an international environment is a plus.
• R and SAS practical and effective knowledge
• Good knowledge of CDISC standards (SDTM and ADaM including specifications)
• Good knowledge of drug development process, industry standards and statistical concepts 

Job Location: Bangalore/ Hyderabad

We are an equal opportunity employer that values workforce diversity. We want everyone to be able to bring their best self to work every day which is why equality and inclusion is at the forefront of all our activities. We are dedicated to a policy of non-discrimination in employment on any basis including race, caste, creed, colour, religion, sex, age, disability, marital status, sexual orientation, and gender identity.

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of our diverse team!