Senior Biostatistician - Clinical Studies
Description:
Be part of a successful and growing Biotech company developing new
generation drugs and medical treatments. Responsible for portions of
major clinical studies projects. This includes statistical integrity,
adequacy, and accuracy of clinical studies projects. Plan, coordinate,
and provides statistical analyses, summaries and reports for product
development and US PLAs/NDAs. Provides appropriate statistical advice
and support to the clinical directors. Adhere to standards of
acceptable statistical methodology, regulatory guidelines and
departmental guidelines.
Requirements:
Ph.D. in Biostatistics or related discipline with 4 plus year’s
experience, or a Master's Degree in Biostatistics with 6 plus years
experience in the support of clinical studies, preferably in a
pharmaceutical industry or clinical studies setting. Knowledge of
applied statistics and biostatistics, and relevant experience in the
applications of statistics to medical trials. Experience with major
statistical software packages such as SAS and S-plus. Strong
interpersonal and effective communication (oral and written) skills.
Experience in phase I-III clinical trials or studies in support of
U.S. PLAs / NDAs.
Email resume for immediate consideration, or for further information
please contact:
Tom Whiting
Enterprise Resource Group
San Francisco, CA
(voice) (415) 221-6300
(email) [EMAIL PROTECTED]
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