m*******s
发帖数: 469 | 1 I have a new position in Greensboro, NC. It’s for Novartis Animal Health
– a very stable company that is working on some interesting projects,
many in the area of vaccines. Ideally they would like to hire at the
Senior Biostatistician level and they are looking for a MS with 3 years
in industry or a PhD with 1. I thought I would circulate this around to
see if you knew anyone who might be interested in such a position –
please feel free to pass it along. Thank you so much! Here is the
official job description:
Supports the Biostatistics Team by providing analysis and interpretation
of study datasets, providing statistical consultation during all phases
of a study. Develops program code for manipulation and analysis of study
datasets, including graphics and tables for the presentation / reporting
of clinical data using SAS and/or other statistical packages.
1. Develops statistical methods and programs, analyzes data, and writes
statistical reports to achieve objectives within given timelines.
2. Advises on the design of titration, pilot, and pivotal efficacy
studies, pilot and pivotal target animal safety studies.
3. Designs, implements, and tests programs for statistical analysis of
assigned studies. Develops tables and graphs for inclusion into
statistical reports, safety reports, Final Study Reports, presentation
slides, and publications.
4. Supports the development and maintenance of the library of SAS (Base,
STAT, Graph, ODS) and other statistical programs. Develops and maintains
a repository of statistical literature.
5. Understands and proactively utilizes knowledge of pertinent local
and/or international Regula-tory Requirements, and may participate in or
lead interactions with local Regulatory Agencies under the guidance of
more experienced Biostatisticians.
6. Attends working groups, conferences, and technical meetings.
7. Collaborates with other associates to facilitate knowledge exchange.
8. Assists in the preparation SOPs related to job function.
9. Works following external and internal guidelines (e.g. SOP’s, GxP,
HSE, AW).
Thank you, as always!
Regards,
Supports the Biostatistics Team by providing analysis and interpretation
of study datasets, providing statistical consultation during all phases
of a study. Develops program code for manipulation and analysis of study
datasets, including graphics and tables for the presentation / reporting
of clinical data using SAS and/or other statistical packages.
1. Develops statistical methods and programs, analyzes data, and writes
statistical reports to achieve objectives within given timelines.
2. Advises on the design of titration, pilot, and pivotal efficacy
studies, pilot and pivotal target animal safety studies.
3. Designs, implements, and tests programs for statistical analysis of
assigned studies. Develops tables and graphs for inclusion into
statistical reports, safety reports, Final Study Reports, presentation
slides, and publications.
4. Supports the development and maintenance of the library of SAS (Base,
STAT, Graph, ODS) and other statistical programs. Develops and maintains
a repository of statistical literature.
5. Understands and proactively utilizes knowledge of pertinent local
and/or international Regula-tory Requirements, and may participate in or
lead interactions with local Regulatory Agencies under the guidance of
more experienced Biostatisticians.
6. Attends working groups, conferences, and technical meetings.
7. Collaborates with other associates to facilitate knowledge exchange.
8. Assists in the preparation SOPs related to job function.
9. Works following external and internal guidelines (e.g. SOP’s, GxP,
HSE, AW).
Let me know if you believe you are qualified. | x*****r
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