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,

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