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Vice President, Clinical Research and Regulatory Affairs The Vice President of Clinical Research
and Regulatory Affairs for this West Coast client will be responsible for all
aspects of clinical development and regulatory affairs on a worldwide basis
for all projects within the company's portfolio. This will involve providing
strategic direction to the clinical research and regulatory functions within
the company, as well as serving as the chief medical spokesperson with all
external parties including investors, principal investigators, key thought
leaders, worldwide regulatory authorities and other appropriate stake
holders. The Vice President will direct the preparation of worldwide
regulatory and clinical development plans and will be responsible for
overseeing the coordination and management of clinical studies in progress,
assuring they will be completed in an acceptable manner and within budget. The successful candidate will have an M.D.
with specialty focus in Cardiology, Oncology or a related field. Ideally, the
successful candidate will be Board Certified in one of the above fields. As
well, at least ten years of clinical research experience in industry with
responsibility for directing a staff is required. [ back ]
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Client Info: Candidate Info: |
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© Copyright 1999 by Caliber Associates. All
rights reserved.
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