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Senior Statistical Programmer

Closing: Jul 10, 2024

This position has expired

Published: Jul 4, 2024 (15 days ago)

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Job Summary

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Requirements:


• 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



Responsibilities

Requirements:


• 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



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

• Interpret project level requirements and develop programming specifications, as appropriate, for complex studies

• Provide advanced technical expertise in conjunction with internal and external clients, and independently bring project solutions to SP teams and Statistical Programming department, for complex studies.

• Fulfil project responsibilities at the level of technical team lead for single complex studies or group of studies.

• Directly communicate with internal and client statisticians and clinical team members to ensure appropriate understanding of requirements and project timelines.

• Estimate programming scope of work, manage resource assignments, communicate project status and negotiate/re-negotiate project timelines for deliverables.

• Provide training and mentoring to SP team members


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