Everest Clinical Research Services,CRO,Clinical Trial,Biostatistics,Programming,Data Management,IWRS,Pharmaceutical,Statistical,Analysis,Inform,SAS,Therapeutic,EDC,Study Portal
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Everest Clinical Research Services Inc. ("Everest") is a contract research organization providing statistical, data management, clinical trial monitoring and medical writing services to pharmaceutical and biotechnology companies. We serve some of the best-known companies worldwide, and work with many of the most advanced drugs in development today. Our Corporate Headquarters is in Markham (Greater Toronto Area), Ontario, Canada with U.S. operations in Little Falls (Greater New York City Area), New Jersey, USA. As we continue to expand our business, we are currently seeking a highly qualified and motivated individual to work in either our Canadian or U.S. office as Associate Director, Statistical Operations.

Associate Director, Statistical Operations

Key Responsibilities:

This is a fantastic opportunity to work with an established biostatistics team, taking some management responsibility for high profile projects. This position is accountable for developing, applying and/or providing expertise in statistical and data management methods and techniques to effectively enable decision making in support of strategies and priorities.

The Associate Director, Statistical Operations will have extensive experience working as a hands on Biostatistician developing clinical trial protocols, writing Statistical Analysis Plans, performing statistical analysis, and generating Statistical and Clinical Study Reports, overseeing the development and implementation of data management and programming work plans and interacting with internal and external clinical trial management personnel.

Additionally, the incumbent will resolve complex problems and provide statistical oversight to other biostatisticians; lead efforts in the development, maintenance and adherence of Corporate policies, SOPs, and therapeutic area specific guidelines; will act as a Lead/Liaison Biostatistician, interacting with clinical trial sponsors and oversee projects in various therapeutic areas.

Qualifications and Experience:

A Ph.D. degree in statistical science plus 10 to 15 years of relevant experience is required for this position.

For this role you must have strong communication skills as you will be working with cross-functional groups. Must have strong technical competence in SAS programming and Statistical sample size calculation software, statistical validation skills and a thorough understanding of statistical principles and clinical trial methodology. Must have a working knowledge of regulatory guidelines relating to statistical analysis, study reports and statistical components of regulatory submissions.

We are an equal opportunity employer. We thank all interested applicants; however, only those selected for an interview will be contacted.

How to Apply

Please send your application, indicating the position to which you are applying to careers@ecrscorp.com.

Posting Date: March 4, 2014

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