Job Description

Senior Programmer I/II

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Purpose

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The role of the Senior Programmer I/II is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas.

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Key Responsibilities

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

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Technical:

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• Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs

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• Author and review simple and complex study TFL shells

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• Author and review straightforward and complex dataset standards

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• Perform data checks and data exploration (e.g. using frequencies, histograms)

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• Program and QC routine and ad hoc datasets and TFLs (in SAS & R) following specifications, applying good programming practice

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• Complete and review CDISC Validation tool reports

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• Ensure the appropriate standards are being applied and adhered to

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• Familiarisation with simple statistical techniques (e.g. t-test, ANOVA, regression, standard survival)

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• Review of project management related documents

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• Maintain study master file documents and any other documents that are required to be audit ready

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Has worked on R and R shiny dashboards.

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Project Management:

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• Act as Lead Programmer and/or Veramed Project Manager for client projects and studies

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• Maintain the project plan

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• Proactive management of resource, scope change and risks

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• Manage the delivery of projects to budget

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• Manage client expectations and issue resolution

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General:

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• Lead internal and client study team meetings effectively

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• Present study updates internally and at client meetings

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• Share scientific, technical and practical knowledge within the team and with colleagues

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• Perform work in full compliance with applicable legislation, regulations, company policies, procedures, and training

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• Build effective collaborative working relationships with internal and client team members

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• Seek opportunities to develop innovative ideas, sharing when appropriate

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• Line management or mentorship of more junior team members

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• Contribution to development of internal training materials

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• Contribution to internal process improvement initiatives

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Minimum Qualification Requirements

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• BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience)

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• At least 4 years of relevant industry experience

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Other Information/Additional Requirements

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• Understanding of clinical drug development process, relevant disease areas, endpoints and study designs

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• Awareness of industry and project standards & ICH guidelines

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• Excellent verbal and written communication skills

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• Interpersonal/teamwork skills for effective interactions

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• Proficiency in data handling using SAS & R

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• Self-management skills with a focus on results for timely and accurate completion of competing deliverables

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• Demonstrated problem solving ability and attention to detail

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• Ability to work independently and as part of a team

📌 Senior Statistical Programmer with R experience (Punjab)
🏢 Veramed
📍 Punjab