| Principal Biostatistician || W2/C2C Contract || Remote at Remote, Remote, USA |
| Email: [email protected] |
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http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=2126525&uid= Hello, Hope you are doing great today. This is Leo Weaver from E-Solutions Inc. Please review the job description if you find yourself comfortable with the description, please share with me your updated resume along with the best time to reach you a quick discussion!! Posting Title: Principal Biostatistician Work Location: Remote Job Type: W2/C2C Contract Job Description: Leverage your statistical expertise and programming skills to execute, manage, and QC synthetic control arm (SCA) projects and further develop innovative approaches to optimize clinical trials. An SCA is an external control created using appropriate statistical methods to achieve baseline balance and to augment clinical trials with patient level data from previous clinical trials. Medidata has access to thousands of previous clinical trials available in the Medidata Enterprise Data Store which may be the basis of this work. Work collaboratively with data standardization subject matter experts, statistical programmers, biostatisticians, and other Medidata groups to assist cross trial integration of historical data and assess adequacy to support project specific research objectives. Create and review protocols, statistical analysis plans, and other clinical trial related documents. Work collaboratively with the statistical programming team to support, develop and review specification for ADaM datasets and perform and guide statistical programmers, and/or QC statistical analysis and reporting of both efficacy and safety clinical trial data utilizing SAS programming. Skills / Requirements: PhD degree or equivalent, in Statistics or Biostatistics. Exceptional candidates with MS degree in Statistics or Biostatistics may be considered 3+ years analyzing and interpreting clinical trials data and/or managing/QCing SAS programming in the Pharmaceutical & Biotech industry. Experience with additional programming languages is a plus. Solid ability in the design, analysis, and interpretation of clinical trials, particularly in time-to-event analyses, propensity score or other matching or weighting methods and/or Bayesian approaches to clinical trials with an appetite for innovation Familiarity with drug development life cycle and experience with the standardization, integration, analysis and reporting of clinical trials data. Regulatory submissions knowledge and experience utilizing define.xml and other submission documents is a plus. Understanding of FDA guidelines. Strong SAS skills and knowledge of CDISC standard. Experience working with and guiding statistical programmers. Experience in Phase II/III Oncology trials a plus Excellent written and verbal ability, including the ability to be persuasive to a technical or non-technical audience Ability to work in a fast paced environment and work on multiple projects at the same time -- Keywords: information technology wtwo microsoft Principal Biostatistician || W2/C2C Contract || Remote [email protected] http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=2126525&uid= |
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| 01:09 AM 30-Jan-25 |