Contract Biostatistician: Date Created : 1/20/2015 11:23:20 AM Category : Biotech/R&D/Science Location/City : PA - Warrington Job Type : Contract Id : 3028838 Were looking for a Sr. Biostatistician with a stable work history and very strong communication skills for a leading Global Biopharmaceutical Company. The senior or contract biostatistician will provide statistical support for clinical/non-clinical development projects and programs. Market Rate, commensurate with education and work experienceInternal Notes: This is a senior level candidate; required 5+ years pharmaceutical industry Biostat experience with Masters degree in statistics or 3 years as a biostatistician if you have Ph.D. in statistics or biostatistics and would not mind to assist in QC SAS coding/etc.If you are interested in aligning with a highly regarded organization that values quality and integrity and fosters an environment where teamwork and professionalism thrive, then dont hesitate to contact us at rchu@gesnetwork or and call Rose Chu, VP in Pharmaceutical & Biotech Services Group at #610-822-1256 for questions. We are always interested in talking to candidates for current AND future opportunities!Please respond directly to Global Employment Solutions, Inc. at rchu@gesnetwork with your resume attached WORD document.SUMMARY: This person will be responsible for statistical contributions to Clinical Study reports, programming of efficacy tables, and statistical analysis. A person in this position will work with SAS programs to analyze and summarize the data, SAS graphs and validation of statistical analyses and findings. Assist in SAS coding/etc.RESPONSIBILITIES: Provides input and review on design of studies, protocols, and case report form (CRF) design; Computes sample sizes in conjunction with clinical staff as required for clinical studies; Writes detailed analysis plans and analyzes clinical data, as directed by immediate supervisor; Designs or oversees the design of summary tables, reports, and graphs for presentation of results; Designs data surveillance plans and analyzes results for trends; Writes statistical analysis descriptions for protocols and final reports, as directed by immediate supervisor; Consults with others in company on statistical issues when requested; Creates and modifies, or directs the creation and modification of, SAS programs to support all of the above; Checks and verifies statistical programs, data listings, and summary tables; Maintains statistical and programming activities and documentation in accordance with Companys policies, procedures and all standard operating procedures (SOPs);Keywords: Statistician, Biostatistician, Clinical Statistician, Statistical Analysis, SAP, Ph.D. Statistics, Ph.D. Biostatistics, Master Statistics, MS Statistics, MS Biostatistics, SAP, SAS, Lead Project Statisticians, biostatistical components, statistical component. Applies statistical, Applied Statistics, Statistical Programming, Biostat, StatKnowledge, Skills, and Competencies Masters or PhD in biostatistics or statistics is required. At least 5 years of pharmaceutical industry experience with Masters degree; at least 3 years of pharmaceutical industry experience with PhD degree. Substantial knowledge of SAS System? programming required; Minimum of three years experience using SAS required; Familiarity with statistical methods used for biomedical/pharmaceutical research required; Experience with clinical trials or pharmaceutical industry experience required; Experience with NDA programs preferred. Knowledge of current industry and regulatory submission practices, protocol designs, and terminology.Other Important Info: A person in these positions will be spending 50% of his/her time on SAS programs to analyze and summarize the data, and the other 50% time on design of the studies and the analysis plan. However, right now they are preparing NDAs (new drug application). There is a heavy workload on statistical programming, so responsibilities will also include SAS graphs and validation of statistical analyses and findings. The group is very busy, and this is a pressing need because of increase in workload. This person will be responsible for statistical contributions to Clinical Study reports, programming of efficacy tables, and statistical analysis.We appreciate your understanding, in that; we will only be able to respond to those inquiries who meet the stated requirements. To protect our clients interests, we will not be responding to inquiries that do not contain a CV/Resume. Finally, please include the position ID (rc-Biostat) in the subject line of your correspondence to ensure review. Please forward your credentials in Word format, in confidence, to: rchu@gesnetwork Our clinical recruiter/manager will contact the qualified candidates IMMEDIATELY to set up interviewsRose Chu Vice PresidentPharmaceutical, CRO, Biotech, Medical DeviceGlobal Employment Solutions, Inc. One Presidential Blvd. North, Suite 310 Bala Cynwyd, PA 19004 610.822.1256 phone 610.822.1210 facsimile rchu@gesnetworklinkedin/in/rosechuReferral Bonus ProgramThe link for registration is: gesnetwork/clinical-ipad-referral-registration dlvr.it/89XWQQ
Posted on: Tue, 20 Jan 2015 19:22:27 +0000
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