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Associate Director MD Open (J#45648)

Title: Associate Director
Company: Kforce

Job Description
Responsibilities: At Kforce Clinical Research, we don't just offer jobs. We offer a rewarding career experience, complete with professional development opportunities and a great benefits package! We are intelligent business partners to some of the world's most valued pharmaceutical companies and have evolved to create models of operational excellence that incorporate Lean and Six Sigma philosophies. Using these tools, Kforce is able to better plan and anticipate work loads and thus minimize the peaks of work that can swamp you. This allows you to stay just as dedicated and still strike a balance between work and home.

Currently, one of our top clients is in search of an exceptional Associate Director of Regulatory Affairs (Oncology) in Gaithersburg, MD. The Associate Director of Regulatory Affairs (Oncology) is responsible for preparing, implementing, communicating, and coordinating regulatory projects, plans and schedules with scientific (clinical and preclinical), manufacturing, and business development project team members for biological products proposed for oncologic indications. The Associate Director of Regulatory Affairs is also responsible for collecting, preparing and assembling documentation required for Investigational New Drug Applications, and Biologic License Applications.
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