ClinChoice
CRO
SeniorManagerBiostatisticianConsultant
“Senior Manager Biostatistician Consultant at ClinChoice. Skills: Biostatistics, Clinical trial experience, SAS programming. Working with study team members and the project statistician to contribute to design of early/late-stage protocols across multiple therapeutic areas. Help draft protocols or amendments”
What You'll Achieve.
Contribute to design of early/late-stage protocols; Perform statistical analyses for interim and final reports; Support submission activities
Industry & Context.
24 months contract
What They're Looking For.
Must Have
MS or PhD in Statistics or Biostatistics, PhD +4 years (or MS +9 years) clinical trial experience in either a biotechnology or pharmaceutical company, Hands-on Phase I/II/III clinical trial experience, Proficient in SAS programming
Nice to Have
Excellence in R programming desirable, Previous experience with regulatory submissions in the US, Europe, Japan, and Rest of the World, is desirable
What You'll Do.
Working with study team members and the project statistician to contribute to design of early/late-stage protocols across multiple therapeutic areas
Help draft protocols or amendments
Develop and write statistical analysis plans
Perform statistical analyses for interim and final reports to be submitted to regulatory agencies
Support submission activities
analysis and reporting of integrated summaries for safety and efficacy
Attendance and statistical contributions at study team meetings
Contribute to the organization and scheduling of study deliverables in collaboration with Statistical Programmers and Data Managers
How You'll Work.
Team & Collaboration
Working with study team members; Attendance and statistical contributions at study team meetings; Collaboration with Statistical Programmers and Data Managers
Communication Scope
Excellent oral and written communication skills
Process & Methodology
Organization and scheduling of study deliverables
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