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Senior/Principal Programmer (R Programmer) Veramed · India
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Veramed

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Senior/Principal Programmer (R Programmer)

🗓️ Posted 2026-09-23 India Hybrid ICT
💰 Salary Not shared 📊 Market ₹150,000–₹350,000/mo

About the Company

Setting the new standard for biometrics to advance the clinical trial process. Veramed is a Clinical Research Organization (CRO) that provides expert data management, biostatistics and programming services to the pharmaceutical and biotech industry. With precision, consistency and an unwavering commitment to quality, Veramed is dedicated to setting the highest standards for biometrics in clinical trials. Founded in 2012, Veramed has always been guided by quality, integrity and humanity. This means a culture that genuinely cares for its employees, and employees that genuinely care about the work they do, enabling unparalleled collaboration for industry-leading delivery. Veramed's growing team of expert data managers, statisticians and statistical programmers supports analysis and consultancy of Phase I-IV clinical trials across a variety of therapeutic areas. Whether it's long-term partnerships or rapid-fire project work, Veramed works as an extension of clients' teams, driving efficient, dependable outcomes. A truly global CRO, Veramed is headquartered in Twickenham, England, with offices across the UK, Europe, US and India. Veramed is proud to be B Corp Certified , committed to integrity and impact in everything we do. Our vision We exist to set the new standard for biometrics. By making the right decisions - for our employees, for sponsors, and for patients - we're redefining what biometrics can deliver in clinical trials. Hear from our team in our podcast: https://veramed.com/resources/ e-filter-bb11a1e-category podcast Research Services Specialties: Statistical Report Writing, SAP's, CDISC Conversion (mapping + back-mapping to SDTM), Data Management Programming, Ad-hoc Programming Services, Statistical Consultancy, Study Design, PRO, Statistics, SAS Programming, Project Management, Resource Management, Data Management, Statistical Programming, Biostatistics

About the Role

statistics and programming department across a range of projects, clients and therapeutic areas. The Principal Programmer may also perform a supervisory role (e.g. line management and/or project management).

Responsibilities

  • ● The job tasks listed below outline the scope of the position. The application of these tasks may vary, based on current business needs.
  • ● Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs
  • ● Author, review and approve study TFL shells and dataset specifications
  • ● Author, validate and document programs for datasets, TFLs and macros, applying good programming practice
  • ● Identify data issues and outliers
  • ● Complete, review and approve CDISC Validation tool reports
  • ● Identify data and standards issues and resolve or escalate as appropriate
  • ● Awareness of emerging standards and associated impact to ongoing and future planned trials
  • ● Maintain proficiency in R and awareness of developments
  • ● Maintain study master file documents and any other documents that are required to be audit ready
  • ● People Management:
  • ● Line management of statisticians, programmer s and other technical staff. Accountable for overall performance of direct reports
  • ● Provide coaching and mentoring of staff to achieve "excellence". Direct employee career development and ensure line reports receive appropriate training to perform their day-to-day jobs
  • ● Interview and effectively on-board and integrate new staff members
  • ● Provide programming technical leadership and coaching
  • ● Project Management:
  • ● Oversight of key client projects/portfolios.
  • ● o Being Veramed Project Manager on client accounts and projects
  • ● o Maintain the project plan
  • ● o Proactive management of resource, scope change and risks