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

^{B.A./B.S. or higher with 5 to 10 years pharmaceutical/ CRO industry relevant experience, of which 3 to 5 years is in Regulatory Affairs.}

^{Experience with IND Amendments.}

^{Experience with NDA Submissions preferred.}

^{Project Management experience.}