Senior Biostatistics Programmer Lead
1 week ago
Company Overview:
TN Ireland's Global Biostatistics team helps interpret and draw inferences from data collected on patients as they progress through a clinical trial and serves as the bridge between data capture and reporting.
We have a collaborative and supportive team environment, where our experts are engaged in the full range of industry-leading resources and expertise spanning all study phases and therapeutic areas.
Job Description:
You will provide experienced technical expertise to develop process methodology for the department to meet internal and external clients' needs.
Key Responsibilities:
- Programming and Development:
- Plan and coordinate the development of integrated programming solutions, serving the full spectrum of statistical programming needs.
- Perform, plan, co-ordinate and implement the following for complex studies: The programming, testing, and documentation of statistical programs for use in creating statistical tables, figures, and listing.
- The programming of analysis datasets (derived datasets) and transfer files for internal and external clients.
- The programming quality control checks for the source data and report the data issues periodically.
Required Skills and Qualifications:
- 5+ years Statistical Programming experience within the Life Science industry
- BSc or MSc degree in Biostatistics or related field
- Experience in SAS Base, and good knowledge of SAS graph and SAS Macros
- Ability to implement more advanced statistical procedures as per specifications provided by Biostatistician.
- Excellent knowledge of CDISC standards (SDTM and ADaM)
- Thorough understanding of relational database components and theory
- Excellent application development skills
- Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis and reporting of analysis results.
- Ability to work on multiple projects, plan, organize and prioritize activities
- Experience as technical team lead directly engaging clients and coordinating tasks within a programming team
- In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Benefits:
- Global exposure
- Variety of therapeutic areas
- Collaborative and supportive team environment
- Access to cutting-edge and innovative, in-house technology
- Excellent career development and progression opportunities
- Work-Life Balance, with a strong focus on a positive well-being
Others:
When you join our diverse, global team, you'll harness the power of unparalleled data, advanced analytics, cutting-edge technologies, and deep healthcare and scientific expertise to drive healthcare forward.
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