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

^{Pharm.D. or B.A./B.S. with at least 2 years relevant industry experience (R.N. with clinical research exposure preferred).}

^{Review clinical data to ensure GCPs; verify all data against source documents.}

^{Project Management experience a plus.}

^{No travel required.}