ASG, Inc., is a nationwide contract consulting firm specializing in the recruitment and placement of Statisticians and SAS professionals in the Pharmaceutical and Biotechnology industries. We currently have a exciting opportunity to be part of a long-term project team working on ?cutting edge? research supporting top clinical client in very attractive location. The primary responsibility of the position is the creation of statistical tables, listings, graphics and derived analysis datasets for final study reports of clinical trials. The statistical programmer is also required to validate his/her own programming code and perform second programmer validation of other programmers? programs. Will assist in the development and validation of integrated databases and the related tables, listings and graphs for integrated safety and efficacy summaries. Requirements: * Minimum BA/BS in scientific, mathematical or computer- related discipline. M.S. is highly preferred, * SAS programming skills of 3-5 years, * At least 2-5 years Statistical programming experience within a clinical trials environment, * Excellent communication skills, * Familiarity with medical/clinical terminology, * Ability to take direction from project Statistician, * Must be capable of reading and understanding the study protocol, Statistical Analysis Plan and documents on study structure and conduct, * Must be experienced in various computer systems (UNIX), and PC-based computer networks, * Must be proficient in SAS programming in Base, Macro, Stat and Graph, * Attention to detail and high standards for producing quality output, ASG offers a flexible compensation plan to include salaried or hourly option, pay for hours worked over 40, 25 paid days offer per year, full medical, dental, life, short-term disability insurance and 401K retirement with 35% employer matching. Kyle Koch Senior Research Recruiter ASG, Inc. 1-800-796-2022 x 20 kyle.koch@asg-inc.com

Biostatistician This client is seeking a highly-qualified Biostatistician to support all aspects of clinical investigation, including design and analysis of clinical studies, collaborate with investigators affiliated with a major medical school, grant and protocol development and review, and teaching and mentoring of junior investigators. The individual must have: *an M.S. or Ph.D. in statistics or Biostatistics *a strong record of collaborative research *3+ years experience *excellent interpersonal skills *excellent oral and written communication *multitasking capability to handle numerous simultaneous projects *a strong commitment to excellence in research. Candidates with broad consulting interests who enjoy collaborating with physicians and research staff are encouraged to apply. Expertise in study design, grant writing, clinical trials, case-control and cohort studies, statistical genetics, hierarchical, longitudinal, survival, nonlinear, SAS. The Biostatistician will have a research associate appointment. and not a clinical trials coordinating center. Interested candidates should send a letter of interest, CV, writing sample, and reference information to resumes@workwondersstaffing.net