Sr Statistical Clinical Programmer (Swiftwater)
Urgent requirement for one of the our top client located in 'PA'. Please contact me at your earliest convenience, along with job No. SCP_PA_90107 to glenn.davis@vernascientific.com. Job Description: The Statistical Programming Manager is responsible for providing significant programming support (SAS software) to the statisticians for statistical analyses and reporting of results of clinical studies. Creates and maintain adequately documented programs to generate analysis files, tables, listings, and graphs in accordance with the Statistical Analysis Plan (SAP) and statisticians’ requirements.Set and maintain professional programming standards, and supports application Platform. development in the Biostatistics Provides programming support to statisticians as appropriate Assists with operational input into Statistical analysis Plan Develops, tests and validates adequately documented programs for randomization scheme, analysis files, production of results tables, listings and figures according to the SAP and statisticians' requirements With supervision by a statistician produces statistical outputs (tables, listings, graphs) included in the Integrated Clinical/Statistical Report (ICSR) Ensures that statistical programs are developed, tested, and validated prior to the target analysis date.Participates, if appropriate, as a member of the Clinical Team accountable to the statistician for all project issues.Provides coaching and mentoring support to Statistical SAS Programmers in the Biostatitics group as appropriate Requirements: Ph.D., with 7 years or more experience, Masters, with 5 years or more experience or Bachelors degree in computer science, statistics, or mathematics and over 10 years experience in the pharmaceutical industry or equivalent qualification/experience. Contact: The most effective way of communication is via email please forward us your updated WORD FORMAT resume (Address, Contact number and email is must) Please mention your best hourly rate, availability and visa status. Any questions, do feel free to email us to glenn.davis@vernascientific.com. About Verna Scientific: Verna is a multidisciplinary Life Sciences firm, Verna specialize in Consulting and Staffing services for Fortune 1000 as well as start-up companies in Biotech, Pharmaceutical and Healthcare industries with major focus on clinical research and data management. Verna is growing rapidly and we are always looking for individuals with outstanding capabilities in clinical arena. We offer careers in both technology and research disciplines. Verna's expertise has earned us an esteemed reputation within the industry and with our clients such as Schering-Plough, Astra Zeneca, Purdue, Abbott Labs, Merck, Wyeth, Allergan and Amgen. Please visit us on the web at www.vernascientific.com Key words: Clinical research associate, clinical research assistant, clinical data manager, clinical research scientist, clinical research coordinator,clinical data analyst, clinical trail manager, clinical project manager, biostatistician, statistical analyst, sas programmer,regulatory affair specialist, regulatory affairs associate, quality analyst, associate director, medical director, senior clinical trail specialist,validation. Compliance, clinical data specialist,statistical programmer, principal,Director
Required Skills: Requirements: Ph.D., with 7 years or more experience, Masters, with 5 years or more experience or Bachelors degree in computer science, statistics, or mathematics and over 10 years experience in the pharmaceutical industry or equivalent qualification/experience.
Desired Skills: With supervision by a statistician produces statistical outputs (tables, listings, graphs) included in the Integrated Clinical/Statistical Report (ICSR)
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