• [Photo] Susan Bernstein February 28, 2002
    Biostatistician
    (2 comments)
    Join a very successful CRO in Los Angeles and provide your technical expertise and programming support for complex clinical trial projects. You will participate on projects as a team player, have an opportunity to really utilize your knowledge, and interact with clients (both internal and external. You will help devise creative solutions and enhance the decision making process.
    You will be responsible for coordination, planning, development, and analysis for SPS tasks which includes analysis file creation, dictionary coding, statistical tables, appendix listings and patient profiles. You will perform necessary departmental quality control procedures and documentation. Serve as technical analyst for programming activities related to complex projects such as NDA or Treatment IND projects, especially during planning stages.

    Please send me a copy of your resume attached as a Word document.
    Susan Bernstein
    Tristaff Group
    858-453-1331
    4350 Executive Drive
    La Jolla, CA 92121
    susan[at]tristaff.com

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Job Opportunity
Submitted by Kyle Koch ; posted on Friday, March 1, 2002
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

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Job Opportunity
Submitted by Kyle Koch ; posted on Friday, March 1, 2002
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

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