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:
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
Work with Data Manager to generate and review database specification documents, CRF specifications, edit checks specifications and data management documents
Program standard and study-specific eCRFs and edit checks in accordance with database specifications and Data Management Plans
Perform data checks as needed to ensure integrity and correctness of data
Create CDISC SDTM datasets and clinical data listings
Perform QC/validation of clinical data listings and edit checks
Supports the development, delivery and maintenance of clinical data review standards, tools and systems
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
US CITIZENSHIP REQUIRED FOR THIS POSITION: Yes RELOCATION ASSISTANCE: Relocation assistance may be available CLEARANCE TYPE: Secret TRAVEL: Yes, 10%...
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