We have an immediate opening for an entry-level Clinical Programmer.
The Clinical Programmer is responsible for performing clinical programming activities for assigned clinical studies. This is a full time on-site position with great career development and advancement opportunities.
Responsibilities:
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Conduct clinical programming to support clinical data management, data cleaning, and data review, as well as external data reconciliation, in accordance with standards/SOPs or study specific guidelines
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Work with Data Manager to generate and review database specification documents, CRF specifications, edit checks specifications and data management documents
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Program standard and study-specific eCRFs and edit checks in accordance with database specifications and Data Management Plans
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Perform data checks as needed to ensure integrity and correctness of data
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Create CDISC SDTM datasets and clinical data listings
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Perform QC/validation of clinical data listings and edit checks
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Supports the development, delivery and maintenance of clinical data review standards, tools and systems
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Perform other duties as assigned
Qualifications:
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Bachelor’s degree or equivalent. Master’s degree in a scientific discipline such as Computer Science, Life Sciences, Statistics, etc. preferred.
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Programming and analytical skills using SAS, R, Python or similar.
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Excellent verbal and written communication skills
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Able to work on multiple, concurrent projects
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A high degree of accuracy and attention to detail
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Knowledge of clinical trial study design a plus
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Employment is subject to a background check