USA - Sr Biostatistician
Posted on :
10-03-2024
Employer Active
1 Vacancy
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Job Description
Req ID : 2610329
Description:
12 months contract
Location Deerfield IL
Hybrid 3 days onsite/ 2 remote no preference on days.
Senior Statistician
What you will be doing at Baxter
Author and/or provide input on statistical sections of clinical study documents including protocols electronic case report forms randomization plans data transfer specifications statistical analysis plans tables listings and figures (TLF) shells SDTM/ADaM specifications clinical study reports and other relevant documents.
Drive TLF development and TLF reviews with programming and other relevant team members determine analysis populations validate key analysis results and present final analysis results to key stakeholders
Accountability for 5 concurrent studies
Represent the Statistics function in study team meetings
What you will bring to Baxter
Masters or PhD in Statistics
35 years recent/related statistical experience within a pharmaceutical and/or medical device company or similar organization
Experience with different clinical phases
Knowledge of clinical trial methodology and study design
Studylevel statistical expertise
Proficiency in SAS and knowledge of CDISC standards
Strong working knowledge of statistical data analysis and data management principles
Senior Statistician
What you will be doing at Baxter
Author and/or provide input on statistical sections of clinical study documents including protocols electronic case report forms randomization plans data transfer specifications statistical analysis plans tables listings and figures (TLF) shells SDTM/ADaM specifications clinical study reports and other relevant documents.
Drive TLF development and TLF reviews with programming and other relevant team members determine analysis populations validate key analysis results and present final analysis results to key stakeholders
Accountability for 5 concurrent studies
Represent the Statistics function in study team meetings
What you will bring to Baxter
Masters or PhD in Statistics
35 years recent/related statistical experience within a pharmaceutical and/or medical device company or similar organization
Experience with different clinical phases
Knowledge of clinical trial methodology and study design
Studylevel statistical expertise
Proficiency in SAS and knowledge of CDISC standards
Strong working knowledge of statistical data analysis and data management principles
Employment Type
Full Time
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