Senior Statistical Programmer (R Programming)

Veramed; India; Vor Ort; INR 2.000.000 - 3.500.000; Vollzeit

Zusammenfassung

Veramed is seeking an experienced Statistical Programmer with R expertise for supporting statistics and programming across multiple clinical studies in India. The role involves programming, data checks, library of SDTM/ADaM standards, and collaboration with internal and client teams.

The candidate should have 7+ years of hands-on statistical programming experience, including R and SAS, and a strong understanding of CDISC standards and clinical trial processes.

Qualifikationen

• 7+ years of hands-on experience in statistical programming.
• Hands-on experience in SDTM, ADaM & TLF.
• Knowledge of CDISC standards and clinical trial processes.
• Experience reviewing protocols, SAPs, CRFs, and CSR documents.
• Proficiency in data handling using SAS or R.
• Understanding of clinical drug development and study designs.

Aufgaben

• Perform programming support to statistics and programming departments across multiple projects and therapeutic areas.
• Author/review study TFL shells and dataset standards.
• Conduct data checks and data exploration (e.g., frequencies, histograms).
• Program and QC datasets and TFLs in SAS per specifications.
• Maintain study master file documents and audit-ready records.
• Lead internal and client study meetings and present study updates.

Kenntnisse

Statistical programming

R programming

SAS

CDISC SDTM/ADaM

TLF

Data checks

ICH guidelines

Ausbildung

Degree in Mathematics/Life Sciences/Statistics/CS

Tools

SAS

R

Jobbeschreibung

We are actively hiring for the role of the Statistical Programmers with R experience (7-12 years) - 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.

Required Skills

• Understanding of clinical drug development process, relevant disease areas, endpoints and study designs
• 5+ Years of hands-on experience in Statistical programming
• Hands-on experience in SDTM, ADaM & TLF
• 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