About the Role
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 easy and complex study TFL shells
Author and review easy 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 positive programming practice
Complete and review CDISC Validation tool reports
Ensure the appropriate standards are being applied and adhered to
Familiarization with easy 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

📌 Senior Statistical Programmer Dombivli
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📍 Dombivli