We have an immediate opening for an entry-level Statistician / SAS Programming Intern with a possibility for a full-time position after the internship and assessment.
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 :
Master’s degree or above in biostatistics or statistics only.3 months of experience with clinical trials or related coursework is required.Able to work on multiple, concurrent projectsA high degree of accuracy and attention to detailKnowledge, Skills, and Abilities :
Proficiency in statistical programming (SAS preferred)Good communication skillsKnowledge of FDA requirements and experience in the pharmaceutical or biotechnology industries is desired.Job Details :
This is a full-time on-site position with great career development and advancement opportunities.
Candidates selected for employment must pass a background check before employment begins.