Location: Bangalore/Hyderabad (Office /Hybrid)

Responsibilities

• Provide project and technical support in the preparation, and review of high-quality programming deliverables and documentation, as well as the processes and standards required, to both colleagues and clients
• Review and provide comments on clinical documents, e.g. protocol, CRF and SAP
• Manipulation of data to produce datasets, including SDTM and ADaMs
• Production and review of Tables, Listings and Figures according to statistical analysis plans
• Creation and review of programming specifications and annotation of case report forms (CRFs) to CDISC standards
• Develop skills of other statisticians or programmers
• Contribute to knowledge share activities
• Deliver excellent customer care
• When required, work as project lead

Skills & Qualifications

• Qualified to degree level or equivalent, preferably in a numerate discipline.
• Experience working within a clinical trials environment
• Experience working with SAS
• Senior Statistical Programmer: 3+ years of relevant work experience
• Principal Statistical Programmer: 8+ years of relevant work experience
• CDISC (SDTM/ADAMS/TLF's) experience
• Good PC skills including working knowledge of Microsoft Office
• Good written and oral communication skills
• Good organisational skills
• Good analytical and problem-solving skills

At Quanticate, our people are our focus, as we understand that they are the key to our success. We strongly believe in work-life balance by offering flexible working arrangements, competitive salary, excellent benefits package and access to tools and computing systems including both SAS and R.