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 Cooridinator

^{Ph.D. or M.S. in scientific discipline or Pharm.D.}

^{Demonstrated expertise with at least 5 years relevant industry experience.}

^{Familiarity with FDA and ICH guidelines.}

^{Ability to prepare, review and present written documents and reports.}

^{At least 2 years experience in preparing clinical reports and/or dossier summary documents (ISS, ISE).}