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 Statistics preferred with at least 5 years pharmaceutical industry experience.  Publications desirable.

Familiarity with FDA, ICH and GCP guidelines.

Ability to review medical and/or scientific data and evaluate protocols and development plans.

Perform statistical analysis and validation.

SAS programming skills required.

Excellent oral communication and writing skills required.



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