Sr. Statistician

is headquartered in Cary, North Carolina (near the university-biotech-pharmaceutical sciences nexus known internationally as Research Triangle Park). Satellite offices strategically placed around the United States, in India and the U.K. underpin Ockham’s global customers and operations.Ockham provides high-quality, global clinical research and strategic development services to pharmaceutical and biotechnology companies, assisting them in the achievement of their strategic planning, technology transfer, licensing, regulatory planning and submissions, pre-clinical development, and manufacturing goals.

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Ockham is a global provider of resources to the Biotechnology and Pharmaceutical Industry. We work with companies involved with clinical trials and other market approval processes to help them deliver their products on time and on budget. One of our clients in California is looking for a . This is a contract position.  This is a Home Based position.

Apply statistical thinking and methods to aid pre-clinical and non-clinical research efforts, in many cases using common statistical methods such as linear and non-linear regression, analysis of variance, non-parametric methods, equivalence testing, and concordance analysis.

This individual will be a member of the Research and Translational Sciences (RTS) Biostatistics team.
Job duties include collaboration with other RTS statisticians and subject matter scientists in planning, designing and analyzing experiments and reporting statistical findings of these experiments, adhering to all Policies, SOPs and other controlled documents.

This individual may also work with RTS statisticians in developing, testing and maintaining automated statistical analysis tools.

If this individual has the interest and expertise, the job duties could include the following:
Writing analysis plans and performing exploratory statistical analyses and modeling for biomarkers in clinical trials; statistical consulting and collaboration for exploratory biomarker analyses; collaborating with other statisticians in Medical Sciences Biostatistics proposing and investigating innovative analyses.

 

Job Requirements 

 

Basic Qualifications:

Masters or Doctoral degree in Statistics/Biostatistics or other subject with high statistical content, and 3 years of post-graduate statistical experience in the pharmaceutical industry or medical research.
Statistical leadership in framing research questions and implementing solutions
Extensive experience in research and translational sciences and/or biomarker analyses
Communication of statistical information (written and oral)
Demonstrated effective communication skills (written and oral)

Keywords: SAS, SAS Programmer, Statistics, Statistical Programmer, Statistical Analysis, ISS/ISE, Biostatistician, Biostatistical Programmer, Clinical Trials, Clinical Research, Clinical Studies, Pharmaceuticals, Drug Development, IND, NDA, Data Management, Data Manager, Clinical Data Manager, Clinical Data Coordinator, Drug Safety, Drug Safety Specialist, Drug Safety Associate, Pharmacovigilence, Drug Safety Nurse, Drug Safety Physician, Medical Writer, Medical Writing, Regulatory Affairs, Regulatory Submissions, Clinical Project Manager, Clinical Trials Specialist, Medical Services Specialist, BSN, RN, Clinical Research Associate, CRA, Clinical Study Manager, Clinical Study Monitor, Clinical Trials Monitoring, Regional CRA, Regional Clinical Research Associate, In-house CRA, In-house Clinical Research Associate, CDISC, SDTM, ADaM, Rave, Medidata, InForm, Home based, telecommuting, ASG, Ockham

 

 

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