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http://biotech.fyicenter.com/jobs/99894999_Senior_Biostatistician.html
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r.com/
Date: 19-Feb-2008
Senior Biostatistician
Specific Responsibilities: Works collaboratively with Statistical
Programmers, Biostatisticians, Clinical Research Associates, Clinical
Data Managers and other Clinical, Global Drug Safety, Regulatory and
Project Management staff to meet project deliverables and timelines
for statistical data analysis and re****ting. Primary responsibilities
include: provides statistical consultation on trial design and study
endpoints, calculates sample sizes and authors statistical analysis
plans, utilizes knowledge of Regulatory requirements and guidance
do***ents to provide statistical advice with respect to creating a
clinical development program, and uses knowledge of literature to
provide data analysis and presentation methods to sup****t publications/
presentations. Works on 4-6 clinical trials / projects as well as
other tasks as assigned by supervisor. Leads a specific component of a
departmental strategic initiative. Knowledge, Experience and Skills :
Typically requires a BS degree in Biostatistics or equivalent and
minimum 6 years of relevant industry experience, or a MS degree in
Biostatistics or equivalent and minimum 4 years of relevant industry
experience in the statistical analysis of biomedical data using SAS=AE
software. Excellent verbal and written communication skills and
interpersonal skills are required. Must have scientific programming
capability with statistical software packages. Analyzes and utilizes
complex information. Anticipates change and reacts quickly and
proactively to accommodate business need. Proactively solicits views
from others to gain common understanding and agreement. Leads by
example and resolves conflict; manages processes for maintaining team
cohesiveness. Uses statistical expertise to demonstrate effective
persuasion. Understands strategic value of information and knows when
and when not to communicate it. Essential Duties and Job Functions:
Works collaboratively with Statistical Programmers, Biostatisticians,
Clinical Research Associates, Clinical Data Managers and other
Clinical, Global Drug Safety, Regulatory and Project Management staff
to meet project deliverables and timelines for statistical data
analysis and re****ting. Primary responsibilities include: provides
statistical consultation on trial design and study endpoints,
calculates sample sizes and authors statistical analysis plans,
utilizes knowledge of Regulatory requirements and guidance do***ents
to provide statistical advice with respect to creating a clinical
development program, and uses knowledge of literature to provide data
analysis and presentation methods to sup****t publications/
presentations. Works on 4-6 clinical trials / projects as well as
other tasks as assigned by supervisor. Leads a specific component of a
departmental strategic initiative. Knowledge, Experience and Skills:
Typically requires a BS degree in Biostatistics or equivalent and
minimum 6 years of relevant industry experience, or a MS degree in
Biostatistics or equivalent and minimum 4 years of relevant industry
experience in the statistical analysis of biomedical data using SAS=AE
software. Excellent verbal and written communication skills and
interpersonal skills are required. Must have scientific programming
capability with statistical software packages. Analyzes and utilizes
complex information. Anticipates change and reacts quickly and
proactively to accommodate business need. Proactively solicits views
from others to gain common understanding and agreement. Leads by
example and resolves conflict; manages processes for maintaining team
cohesiveness. Uses statistical expertise to demonstrate effective
persuasion. Understands strategic value of information and knows when
and when not to communicate it.
Thank you,
BioTech FYI Center
http://biotech.fyicenter.com/
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