About the Role
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The Statistical Programmer role is primarily responsible for supporting statistical programming tasks on one or more clinical studies under the supervision of more senior Statisticians.
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Responsibilities
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1. Develop and maintain SDTM and ADaM or analysis datasets specifications for assigned projects.
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2. Program SDTMs, ADaMs or analysis datasets, tables, figures, and listings (TFLs) according to approved specifications.
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3. Adhere to company statistical programming standards and conventions, and data standards.
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4. Ensure that SAS programs generated for data storage, transformation, presentation, and statistical analysis are properly documented and traceable.
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5. Maintain study documentation, programs, and files within project files and maintain timesheets.
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6. Ensure compliance with applicable regulatory agency guidelines and corporate policies and SOPs, and SOPs for study design, protocol development, and all other statistical programming output.
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7. Minimum Bachelor's Degree with concentration in Life Sciences, Computer Science, Mathematics, Statistics or in Quantitative/Analytical field.
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8. Basic knowledge of Base SAS. Good organizational and communication skills.
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9. Able to perform work independently while able to establish and maintain effective working relationships with coworkers, managers, and clients.
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10. Passionate about working in clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.
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11. Flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs, and ongoing development programs.
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We look forward to contacting you regarding your application.