Statistical Consultant
•Review and contribute to study protocols, statistical analysis plans, and clinical study reports, adhering to regulatory guidelines and industry best practices.
•Develop and implement advanced statistical methodologies and models, ensuring appropriate implementation to address project needs in one or more Therapeutic or Technology Areas.
•Analyze and interpret clinical trial data, including efficacy and safety endpoints, and provide actionable insights to support decision-making.
•Collaborate with statisticians, data scientists, and programmers to ensure the accurate and timely delivery of statistical outputs for regulatory submissions and scientific publications.
•Conduct exploratory data analysis, including use of visualization and statistical techniques to identify trends, patterns, and potential safety signals in clinical trial data.
•Participate in meetings with regulatory authorities, addressing statistical queries and providing necessary documentation for submissions.
Minimum Requirements
•Advance degree in Statistics or related discipline
•At least 3 years' experience supporting the design and analysis of clinical trials in a Medical Device or Pharmaceutical company
•SAS programming experience is a must, R programming experience is a plus
Custom Fields:
Name: Invoice Type
Value: USA-ARL-Staffing-USD
Name: System Access Required
Value: Yes
Name: Remote Worker
Value: No
Name: Supervisory Org
Value: Statistics 03(Trina Patel)-10084440
Name: Work Desk Phone Number Required
Value: No
Name: Workspace
Value: None
Name: Badge ID Required
Value: Yes
Name: Worker Time Type
Value: Full Time
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