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

^{Ph.D. or M.S. in chemistry or pharmacy, or Pharm.D. with at least 3 years relevant industry experience.}

^{Experience in preparation and review of CMC sections of documents, reports, and regulatory submissions.}

^{Familiarity with FDA and ICH guidelines.}

^{Project Management experience a plus.}