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

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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.



One Main Street  Chatham, NJ 07928 USA  Phone: 1.973.635.9898  Fax: 1.973.635.9881