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Senior Biostatistician Tell A Friend   Organization: Clinical and Systems Resource Group View Company Profile of Clinical and Systems Resource Group :: View more jobs from Clinical and Systems Resource Group Job Description: The Statistician is responsible for providing statistical analyses and summaries of studies in support of product development and PMA, BLA and NDA submissions. He/she will review the statistical analysis sections of clinical protocols, write statistical analysis plans, prepare table and listing shells, create randomization schedules, review CRFs and Data Management Plans, and conduct statistical analyses. The Statistician will work with SAS programmers and provide specifications of necessary analyses and summaries. He/she will be responsible for developing SAS programs and overseeing quality control activities to ensure the accuracy of the final results summaries produced by the SAS programmers. The company is a contract research organization that provides clinical data management and statistical services to the Biotech, Pharmaceutical, and Medical Device industries. We are a growing company of 60 providing a small company atmosphere and opportunity for career development. The expertise we provide leads to the submission of clinical trials data to the FDA and other regulatory agencies around the world. We are currently seeking both a full-time Statistician and Senior Statistician. advertisement Skills Required: Job Duties/Responsibilities: - Responsible for providing statistical Analyses and summaries of studies in support of product development and BLAs/NDAs. - Review statistical analyses sections of clinical protocols, write analysis plans, create randomization schedules, review CRF’s and Data Management Plans. - Responsible fro Accuracy of final results of SAS Programmers. - Experience with Data from Phase 1-3 Clinical trials a must Qualifications: Education, Experience, and Other Requirements: - Requires an MS in Statistics or related field - 1-4 years of experience (3-10 for Senior Statistician) working in an environment that requires the ability to set priorities and meet deadlines. Experience with statistical analysis of data obtained from phase I-III clinical trials or studies in support of PMAs/BLAs/NDAs. - Experience supervising statistical staff is a plus - Requires strong statistics skills, experience with major statistical software packages such as SAS and S-plus - Excellent analytical, problem solving, organizational, interpersonal and communication skills, and proficiency in various software applications such as MS Word, Excel, etc. Job Category: Biotechnology Job Status: Full Time Location: San Francisco, United States Start Date: ASAP Salary: 80,000 - 120,000 Contact: Andrew Mammano Email: Andrew@srgr.com Reference: Snr Biostat Date Posted: 8/28/2008 6:57:22 PM Duration: