Job Description
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 projects
- A high degree of accuracy and attention to detail
Knowledge, Skills, and Abilities:
- Proficiency in statistical programming (SAS preferred)
- Good communication skills
- Knowledge 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.
Job Tags
Full time, Internship, Immediate start,