Qualified Applicants will possess:

Statistician

Physician

Project Manager

SAS Programmer

Clinical Research Associate

Scientific / Medical Writer

Pharmacologist / Pharmacokineticist / Toxicologist

Pharmaceutical Chemist

Director / Manager, Regulatory Affairs

Regulatory Submission Specialist / Document Coordinator

^{M.S. preferred with at least 10 years pharmaceutical industry experience in programming.}

^{Design/prepare/validate databases, analyses, datasets and documentation.}

^{Expertise in SAS required; Oracle and Access/VBA a plus.}

^{Ability to manage projects preferred.}

^{Interest in expanding knowledge and training others.}