Qureos Mentor

LLX Solutions

<div>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: 
<ul><li>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</li><li>Work with Data Manager to generate and review database specification documents, CRF specifications, edit checks specifications and data management documents</li><li>Conduct clinical programming to create data sets, tables, figures, and listings for reports</li><li>Perform data checks, program/document validation as needed to ensure integrity and correctness of data</li><li>Support the development, delivery and maintenance of clinical data review standards, tools and systems</li><li>Responsible for documentation to support the programming and inspection</li><li>Perform other duties as assigned</li></ul>
 
Qualifications: 
<ul><li>Master&rsquo;s degree or above in biostatistics or statistics only.</li><li>3 months of experience with clinical trials or related coursework is required.</li><li>Able to work on multiple, concurrent projects</li><li>A high degree of accuracy and attention to detail</li></ul> 
Knowledge, Skills, and Abilities: 
<ul><li>Proficiency in statistical programming (SAS preferred)</li><li>Good communication skills</li><li>Knowledge of FDA requirements and experience in the pharmaceutical or biotechnology industries is desired.</li></ul> 
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.</div>

Statistician/SAS Programming Internship

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Statistician/SAS Programming Internship