Senior Statistical Programmer (R Programming)

Veramed; India; On-site; INR 1,200,000 - 1,800,000; Full time

Job summary

Veramed in India is seeking a Senior Programmer I to support statistics and programming across projects and therapeutic areas. You will review protocols, SAPs, CRFs, CSR documents and generate SAS datasets and TFLs, while ensuring CDISC standards.

The role requires 5+ years of experience, strong SAS/R skills, and the ability to work both independently and in a team, with opportunities for mentorship and process improvement.

Qualifications

• Degree in Mathematics, Life Sciences, Statistics, or Computer Science.
• Minimum 5+ years of relevant industry experience.
• Strong SAS programming with SDTM, ADaM, and TFL development.
• Good knowledge of CDISC standards and clinical trial processes.
• Hands-on experience in R programming and data handling with SAS/R.
• Awareness of ICH guidelines and industry standards.
• Demonstrated problem solving and attention to detail.
• Ability to work independently and in a team.
• Excellent verbal and written communication skills.

Responsibilities

• Perform consistency review of clinical trial documents and programs.
• Author and review SAS SDTM/ADaM/TFL components.
• Prepare data checks and exploratory analyses (frequencies, histograms).
• Program and QC datasets and TFLs per specifications.
• Review CDISC Validation tool reports and ensure standards adherence.
• Lead internal and client study team meetings and present updates.
• Mentor junior team members and contribute to training materials.

Skills

SAS programming

R programming

CDISC standards

TFL development

SDTM/ADaM

Data handling

ICH guidelines

Team mentorship

Communication skills

Education

Degree in Mathematics, Life Sciences, Statistics, Computer Science

Tools

SAS

R

Job description

We are actively hiring for the role of the Senior Programmer I - this role is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas.

The job tasks listed below outline the scope of the position. The application of these tasks may vary, based on current business needs.

Responsibilities

Technical:

• Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs
• Author and review simple and complex study TFL shells
• Author and review simple and complex dataset standards
• Perform data checks and data exploration (e.g. using frequencies, histograms)
• Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice
• Complete and review CDISC Validation tool reports
• Ensure the appropriate standards are being applied and adhered to
• Familiarization with simple statistical techniques (e.g. t-test, ANOVA, regression, standard survival)
• Review of project management related documents
• Maintain study master file documents and any other documents that are required to be audit ready

General:

• Lead internal and client study team meetings effectively
• Present study updates internally and at client meetings
• Share scientific, technical and practical knowledge within the team and with colleagues
• Perform work in full compliance with applicable legislation, regulations, company policies, procedures, and training
• Build effective collaborative working relationships with internal and client team members
• Seek opportunities to develop innovative ideas, sharing when appropriate
• Line management or mentorship of more junior team members
• Contribution to development of internal training materials
• Contribution to internal process improvement initiatives

Qualifications

• Degree in a relevant field such as Mathematics, Life Sciences, Statistics, Computer Science, etc.
• At least 5+ years of relevant industry experience

Required Skills

• Understanding of clinical drug development process, relevant disease areas, endpoints and study designs
• Strong SAS programming skills with SDTM, ADaM, and TFL development experience
• Good knowledge of CDISC standards and clinical trial processes
• Experience reviewing protocols, SAPs, CRFs, and CSR documents
• Hands on experience in R Programming.
• Proficiency in data handling using SAS or other statistical software (e.g. R)
• Awareness of industry and project standards & ICH guidelines
• Demonstrated problem solving ability and attention to detail
• Ability to work independently and as part of a team
• Excellent verbal and written communication skills
• Interpersonal/teamwork skills for effective interactions
• Self-management skills with a focus on results for timely and accurate completion of competing deliverables

Equal Opportunity Statement

We are committed to diversity and inclusivity.

About Veramed:

Veramed is a biometrics-focused CRO, primarily specializing in Statistics and Statistical Programming. Recently, we have also started expanding into Data Management and are in the process of building dedicated data management teams across the UK, US, and India. The company was founded in 2012 by Matthew Jones, a Statistical Programmer, and Emma Jones, a Statistician. Over the past 13 years, Veramed has grown significantly and now has a global workforce of around 750-800+ employees. We have a strong international presence, with three offices in the UK, two offices in Ukraine, and teams located in Spain, Germany, France, and the United States. In India, we launched our operations in March 2024, and within just two years we have grown to 170 employees, including contractors. Currently, we have an office in Bangalore, and our second office in Hyderabad will be launching soon. One of our key strengths is our employee retention, with a strong retention rate of around 92–93% globally. This role offers an excellent opportunity to work alongside experienced professionals, contribute to meaningful clinical research projects, and further develop your technical and programming skills in a collaborative environment