Qualified Applicants will possess:

Statistician

Physician

Project Manager

SAS Programmer

Clinical Research Associate

Scientific / Medical Writer

Pharmacologist / Pharmacokineticist / Toxicologist

Pharmaceutical Chemist

Dierctor / Manager, Regulatory Affairs

Regulatory Submission Specialist / Document Coordinator

^{At least 2 years relevant industry experience.}

^{Familiarity with FDA and ICH guidelines.}

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

^{Project Management experience a plus.}

^{Safety Surveillance experience a plus.}