Date: 02-Jan-2014
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Scientist I, Clinical Pharmacokinetics
Responsible for preparation of reports for studies with PK and PK/PD aspects, CSR, and review and finalization of reports
Assemble data sets for WinNonlin and NONMEM
Independently perform non-compartmental analysis
Responsible for preparation of PK, PK/PD components of internal documents, briefing books, and regulatory submission documents (e.g. IND, NDA, IB and other regulatory documents)
Collaborate with Clinical Pharmacology project leaders and other colleagues to generate abstracts and manuscripts for publication
Master's (MS) with 5 plus years of relevant industry experience or Ph.D. with 0-2 years of relevant industry (or post-doctoral) experience in pharmacokinetics, pharmaceutical sciences, biological sciences, biostatistics, or related field
Strong analytical and programing skills
Ability to evaluate and interpret standard pharmacokinetic and pharmacodynamic scenarios and prepare PK reports
A good working knowledge of Phoenix WinNonlin
Familiarity with Microsoft Office, Excel, Power Point, and SigmaPlot graphics
Expertise with SPlus, basic SAS programming, and R
Excellent writing and effective communication skills.
Proven interpersonal, organizational and problem solving skills in a matrix management environment
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BioTech FYI Center
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