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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Ph.D. in scientific discipline.

Demonstrated expertise with at least 2 years relevant industry experience.

Familiarity with FDA and ICH guidelines.

Ability to prepare, review and present written documents and reports.

Project Managment experience a plus.



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