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. and/or 3 years pharmaceutical/CRO experience in document management.}

^{Proficiency in MS Word and PC skills.}

^{Ability to prepare submissions in accordance with analysis plans and industry and regulatory guidelines.}