Sr. Statistician in Cambridge, IL at DISYS

Date Posted: 6/22/2018

Job Snapshot

Job Description

Hi,



Greetings From DYSIS!!!



My name is Aravind. I represent the Talent team within DISYS (www.disys.com).  DISYS is a global technology and business services consulting firm specializing in Business and IT Consulting & Staffing Services to commercial and government customers.  We are a $350 million private firm with 20 branches in the US and 13 international locations servicing over 200 Fortune 1000 clients.



If you are interested in the below position, feel free to reach me.



Title                         - Sr. Statistician


Location                 - Deerfield, IL & Cambridge, IL.


Contract                 - 12+ Months


 


Job Description:


Objectives:


•       Participate in designing, analyzing and interpreting data from clinical studies.


•       Use standards to maximize global data integratability and interpretability.


•       Interact with internal and external resources to achieve quality, timely and cost-effective study deliverables.



Accountabilities:


•       Represent the statistics function in support of a clinical study, Partner with clinicians, relevant team members and other statisticians to design efficient clinical trials.


•       Develop efficient analysis methodologies and responsible for completion of statistical analysis plan.


•       Conduct modeling and simulations with minimal supervision.


•       Provide statistical support in the development and review of study synopsis, protocol, clinical study report, and regulatory submission documents.


•       Implement project level database, analysis and reporting standards. Provide suggestions to achieve high quality.


•       Databases and specifications by working with Data Management, Programming and other functions at study level.


•       Plan, direct or self-implement study-level analysis and reporting activities (e.g. tables, listings, graphs) including review of work from other programmers.


•       Provide technical oversight of statistical activities of external vendors to ensure timeliness and quality of analysis data and statistical outputs. Review and approve key statistical vendor deliverables.


•       Anticipate and communicate study level resource and quality issues that may impact deliverables or timelines. Propose and implement solutions. Escalate issues to management as appropriate.



Education, Experience, Knowledge and Skills:


•       PhD in statistics or biostatistics (entry level) or MS in statistics or biostatistics with minimum of 3 years of relevant experience.


•       Good understanding of clinical study designs and analysis methodologies.


•       Knowledge of the pharmaceutical industry including understanding of clinical drug development process and associated documents.


•       Familiar with FDA and ICH regulations and industry standards applicable to the design and analysis of clinical trials.


•       Strong programming skills using SAS and other statistical software.


•       General project management skills at study level.


•       Good oral and written communications skills.


•       Good collaborative skills and ability to work with a cross-functional team




Warm Regards,


Aravindarajan


Technical Recruiter


Digital Intelligence Systems (DISYS)


Phone: 972-776-6775  | www.disys.com


Email: aravind.pandiarajan@disys.com

Job Requirements

Hi,



Greetings From DYSIS!!!



My name is Aravind. I represent the Talent team within DISYS (www.disys.com).  DISYS is a global technology and business services consulting firm specializing in Business and IT Consulting & Staffing Services to commercial and government customers.  We are a $350 million private firm with 20 branches in the US and 13 international locations servicing over 200 Fortune 1000 clients.



If you are interested in the below position, feel free to reach me.



Title                         - Sr. Statistician


Location                 - Deerfield, IL & Cambridge, IL.


Contract                 - 12+ Months


 


Job Description:


Objectives:


•       Participate in designing, analyzing and interpreting data from clinical studies.


•       Use standards to maximize global data integratability and interpretability.


•       Interact with internal and external resources to achieve quality, timely and cost-effective study deliverables.



Accountabilities:


•       Represent the statistics function in support of a clinical study, Partner with clinicians, relevant team members and other statisticians to design efficient clinical trials.


•       Develop efficient analysis methodologies and responsible for completion of statistical analysis plan.


•       Conduct modeling and simulations with minimal supervision.


•       Provide statistical support in the development and review of study synopsis, protocol, clinical study report, and regulatory submission documents.


•       Implement project level database, analysis and reporting standards. Provide suggestions to achieve high quality.


•       Databases and specifications by working with Data Management, Programming and other functions at study level.


•       Plan, direct or self-implement study-level analysis and reporting activities (e.g. tables, listings, graphs) including review of work from other programmers.


•       Provide technical oversight of statistical activities of external vendors to ensure timeliness and quality of analysis data and statistical outputs. Review and approve key statistical vendor deliverables.


•       Anticipate and communicate study level resource and quality issues that may impact deliverables or timelines. Propose and implement solutions. Escalate issues to management as appropriate.



Education, Experience, Knowledge and Skills:


•       PhD in statistics or biostatistics (entry level) or MS in statistics or biostatistics with minimum of 3 years of relevant experience.


•       Good understanding of clinical study designs and analysis methodologies.


•       Knowledge of the pharmaceutical industry including understanding of clinical drug development process and associated documents.


•       Familiar with FDA and ICH regulations and industry standards applicable to the design and analysis of clinical trials.


•       Strong programming skills using SAS and other statistical software.


•       General project management skills at study level.


•       Good oral and written communications skills.


•       Good collaborative skills and ability to work with a cross-functional team




Warm Regards,


Aravindarajan


Technical Recruiter


Digital Intelligence Systems (DISYS)


Phone: 972-776-6775  | www.disys.com


Email: aravind.pandiarajan@disys.com

Digital Intelligence Systems, LLC. is an Equal Opportunity Employer, M/F/D/V. We do not discriminate against any employee or applicant because they inquired about, discussed, or disclosed compensation. Email recruitinghelp @ disys.com to contact us if you are an individual with a disability and require accommodation in the application process.

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