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

^{B.A./B.S. and at least 2 years pharmaceutical/CRO experience with strong organizational and analytical skills.}

^{Develop project plans, timelines and budgets for projects.}

^{Experience in project management (Phase I-IV).}

^{Working knowledge of technical documents including clinical trial reports, INDs and NDAs.}

^{Experience with MS Project required.}

^{Capacity planning experience required.}