Job titleBiostatistician EmployerEverest Clinical Research Services Inc.Job TypeFull Time Salarynot disclosed LocationMarkham , Ontario Date Posted08/01/2013 - 15:45 Closing Date 31/01/2013 - 15:45 PAST CLOSING DATE Job DescriptionSummary: 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 Toronto (Markham), 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 highly qualified and motivated individuals to work in either our Markham, Ontario and our Little Falls, New Jersey office as BIOSTATISTICIANS. Education & Qualifications: We require a Ph.D. degree in statistical science plus 1 to 2 years of relevant experience or a master’s degree plus 4 to 5 years relevant experience with demonstrated ability and sustained performance. Experience: The incumbent must have the ability to lead project teams, strong technical competence in statistics and SAS programming, as well as working level knowledge of data management are essential for the success of this position. Intensive SAS programming for statistical analysis and the generation of statistical tables, listings a, and graphs will be a requirement. Hands on key data management activities such as participation in writing of Data Management Plan, reviewing of data queries, and cleaning up databases, will also be a requirement. Solid understanding of clinical drug development process and knowledge of FDA regulatory requirements and ICH/GCP guidelines is preferred. Duties & Responsibilities: The Biostatistician will be a leader for statistical and data management projects, providing both leadership skills as well as technical expertise to the project teams. The incumbent will participate in developing clinical study protocols, write Statistical Analysis Plans, perform statistical analyses, and generate Statistical and Clinical Study Reports. The Biostatistician will also oversee the development and implementation of data management and programming work plans, interact with internal and external clinical study management personnel to jointly achieve clinical study objectives and timelines. Other Information: Please send your application, indicating the position to which you are applying to email@example.com. We are an equal opportunity employer. We thank all interested applicants, however, only those selected for an interview will be contacted.