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Senior Biostatistician

Overview
Starting over 25 years ago, we have grown into one of the most successful global IT consulting companies with offices spanning several countries. We are both strategic advisors and full service IT providers with a comprehensive know-how under one roof. Our customers core business benefit from us optimizing their business processes and efficiently implemented their technology investment. We've established ourselves by creating perfect system architectures supported by the best equipment available. Our shared goal is to facilitate seamless IT processes that enable our customers to simply focus on their business without interruption.
We are seeking a Senior Biostatistician to join our fast growing and dynamic global IT consulting company.
Principal responsibilities:

  • Provide statistical input into the clinical development of drugs for treatment of cancer.

  • Work with the clinical team in designing clinical studies, leading/authoring the statistical analysis plan, conducting the statistical analysis, and providing statistical input to the clinical study report.

  • Provide input in the preparation of scientific presentations and manuscripts.

  • Participate in process improvement, training, standards development and enhancing statistical technical expertise.

  • Liaise with other statisticians within the organization, building working relationships with therapeutic area leaders, internal SAS programmers, clinical trial managers, and personnel from regulatory affairs, medical writing, and other disciplines as needed.

  • Work with external partners including key opinion leaders in the oncology area, may work with external regulatory agencies and advisory committees, and contract research organizations.


Qualifications:

  • A Master's degree in Statistics or related field with at least 4 years of clinical data analysis experience is required OR a PhD in Statistics or related field is preferred.

  • Working knowledge of statistical software such as SAS, R, or SPlus is required.

  • Experience and knowledge of Good Clinical Practices and regulatory requirements for clinical drug development, including the conduct of clinical trials is preferred.

  • Excellent verbal and written communication skills, including formal presentation skills are required.

  • Experience presenting to technical and lay groups at public meetings is preferred.

  • Advanced knowledge of statistical methodology including experience with modeling and simulations is preferred.

  • Excellent analytical skills are required.

  • Up to 10% travel is required.


Benefits Overview
Competitive salary and benefits packages
Company Description:

Starting in Switzerland 25 years ago, redtoo inc. has grown into one of the most successful global IT consulting companies with offices spanning several countries. We are both strategic advisors and full service IT providers with a comprehensive know-how under one roof. Our customers core business benefit from us optimizing their business processes and efficiently implemented their technology investment. We've established ourselves by creating perfect system architectures supported by the best equipment available. Our shared goal is to facilitate seamless IT processes that enable our customers to simply focus on their business without interruption.




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