Medidata: Power Smarter Treatments and Healthier People
Medidata is leading the digital transformation of life sciences, creating hope for millions of patients. Medidata helps generate the evidence and insights to help pharmaceutical, biotech, medical device and diagnostics companies, and academic researchers accelerate value, minimize risk, and optimize outcomes. More than one million registered users across 1,900+ customers and partners access the world's most trusted platform for clinical development, commercial, and real-world data. Medidata, a Dassault Systèmes company, is headquartered in New York City and has offices around the world to meet the needs of its customers. Discover more at www.medidata.com and follow us @medidata.
Medidata is looking for individuals who will help us tackle some of the most complex questions facing the industry today using our proprietary platform and advanced analytics. At Medidata, we never work alone. This role will partner heavily with all of the key stakeholder functions including product, delivery, data science, engineering, partnerships, and biostatistics. Successful Medidata AI candidates will be skilled in analytical/quantitative thinking, structured communication, and excited about building the next horizon of Medidata’s mission to power smarter treatments and healthier people.
Who We're Looking For:
Provide statistical expertise for the development and support of innovative approaches to optimize the conduct and science of clinical trials, including use of synthetic control arms.
Leverage your statistical expertise and advanced programming skills to execute, manage and QC customer synthetic control arm projects and further develop innovative approaches to optimize clinical trials.
Create and review protocols, statistical analysis plans, and other study related documents. Work with the programming team to support, develop and review specification for different datasets, including SDTM/ADAM.
Work collaboratively with data standardization subject matter experts, statistical programmers and biostatisticians and other Acorn AI groups to assist in evaluating the accuracy of integrated historical data
Perform, guide statistical programmers, and/or QC statistical analysis and reporting of clinical trial data, both safety and efficacy, utilizing SAS programming
Solid ability in the design, analysis, and interpretation of clinical trials, particularly in 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 manipulation, analysis and reporting of clinical trials’ data.
Regulatory submissions knowledge and experience utilizing define.xml and other submission documents. Understanding of FDA guidelines.
Strong SAS skills.
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
Requirements (Education & Experience):
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 working with and guiding statistical programmers
Experience in additional programming languages and/or Oncology trials preferred
The salary range posted below refers only to positions that will be physically based in New York City. As with all roles, Medidata sets ranges based on a number of factors including function, level, candidate expertise and experience, and geographic location. Pay ranges for candidates in locations other than New York City, may differ based on the local market data in that region. The base salary pay range for this position is $157,500 to $210,000.
Base pay is one part of the Total Rewards that Medidata provides to compensate and recognize employees for their work. Most sales positions are eligible for a commission under the terms of applicable plan documents, while many of Medidata’s non-sales positions are eligible for annual bonuses. Additionally, Medidata provides best-in-class Benefits. We believe that benefits should connect you to the support you need when it matters most and should help you care for those who matter most. For that reason, we provide an array of options to help support you physically, financially and emotionally through the big milestones and in your everyday life.
MEDIDATA generates the evidence and insights to help pharmaceutical, biotech, medical device and diagnostics companies, and academic researchers accelerate value, minimize risk, and optimize outcomes.