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| Req. #: |
11709 |
Position: |
Lead Analyst |
| Business: |
Pharmaceuticals |
Contact: |
John Giornalista 908-709-9800 |
| Location: |
Nutley, NJ |
Duration: |
Permanent |
Project Description: |
Our client in NJ seeks a full time Lead Analyst.
Responsibilites:
- provide oversight to assigned SAS programmers for the project, both internal and contract;
- participate as a member of Study Management Teams and assist in the development of case report forms, data validations, and data quality plans;
- lead the development and documentation of mapping specifications for the creation of standard analysis data sets;
- act as contact person within Biostatistics dealing with Data Management;
- implement report specifications as defined in statistical analysis plans and respond to ad-hoc requests to produce reports for Clinical customers (tables, listings and graphs);
- design robust, flexible, and modular software for the project;
- direct team members in creation of individual components;
- oversee integration testing of the entire project software suite;
- administer standard validation requirements by: managing code reviews, applying a development-QA-production code development lifecycle, authoring and/or reviewing validation plans and reports;
- act as contact person within Biostatistics dealing with the exporting of data to the Electronic Submissions group as well as others dealing with Genetics and Pharmacoeconomics;
- act as contact person within Biostatistics with outside companies on data and programming issues;
- maintain up-to |
Required Skills: |
- Qualified candidates must possess a B.S./B.A. in computer science, mathematics, statistics or related areas of study.
- In-depth knowledge of SAS programming with at least 5 years of experience in a pharmaceutical industry biostatistics environment.
- Strong knowledge of SAS Macro.
- Knowledge of clinical data processing, with emphasis on regulatory agency requirements for data reporting.
- Understanding of data and system dependencies, experience in integration of studies (ISE and ISS) and validation techniques.
- Knowledge of UNIX (including basic shell scripting) and experience leading other programme |
Other Information: |
- High level of accuracy and attention to detail.
- Ability to work in a team environment and good communication skills |
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