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Biostatistician Details
Typical Biostatistician duties and responsibilities include:
Job Description: This position is
responsible for biostatistical activities in support of clinical trials including:
generating data tables, patient data listings and reports using SAS; preparing statistical
analysis plans; contributing
to the statistical section of clinical trial protocols;
reviewing analysis of clinical trial data.
Responsibilities:
- Generates statistical summary tables, patient data listings
and reports using SAS.
- Performs quality control check of SAS programs.
- Handles basic SAS programming issues as well as all
other study programming issues.
- Assists with UAT of SAS dataset transfer files.
- Works with the Biostatistics Manager and Clinical Sciences
staff to develop scientifically sound clinical study designs and contributes to
the statistical section of clinical research protocols.
- Contributes to or prepares statistical analysis plans
under the direction of the Biostatistics Manager.
- Prepares template and performs programming for periodic
progress reports for assigned clinical programs.
- Compiles clinical data and relevant background material,
and presents these results to the Biostatistics Manager for review.
Qualifications:
- Master's level degree in biostatistics, statistics,
or public health; Bachelor's level degree will be considered.
- At least 1 year of experience in SAS programming; preferably
1 year in medical device or pharmaceutical clinical trials.
- Demonstrated
computer expertise in SAS programming and
word processing; experience using SQL and EDC highly desirable.
- Familiarity with clinical trial design and analysis
issues.