Job Description

Responsibilities:  

• Conduct clinical programming to support clinical data management, data cleaning, and data review, as well as external data reconciliation in accordance with standards (CDISC, MedDRA, WHO-DD, FDA)/SOPs or study specific guidelines 
• Work with Data Manager to generate and review database specification documents, CRF specifications, edit checks specifications and data management documents 
• Conduct clinical programming to create data sets, tables, figures, and listings for reports 
• Perform data checks, program/document validation as needed to ensure integrity and correctness of data 
• Support the development, delivery and maintenance of clinical data review standards, tools and systems 
• Responsible for documentation to support the programming and inspection 
• Perform other duties as assigned 

Qualifications:  

• Bachelor’s degree or equivalent. Master’s degree in a scientific discipline such as Computer Science, Life Sciences, Statistics, etc. preferred. 
• Programming and analytical skills using SAS, R, Python or similar. 
• Excellent verbal and written communication skills 
• Able to work on multiple, concurrent projects 
• A high degree of accuracy and attention to detail 
• Knowledge of clinical trial study design a plus 
• Employment is subject to a background check 

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