Vice President, Clinical Development and Regulatory Affairs The Vice President of Clinical Development and Regulatory Affairs for this start-up company based in New England 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 individual will direct the preparation of worldwide regulatory and clinical development plans. The Vice President will be responsible for building the clinical and regulatory functions as appropriate, and directing the activities of all pertinent external consultants and collaborators. The Vice President will serve as the key company spokesperson on all issues pertaining to clinical studies. The successful candidate will have an M.D. with a specialty focus in Oncology, Immunology or Infectious Diseases, with Board Certification in one of the above fields highly desired. As well, at least ten years of clinical research experience in industry with responsibility for directing a staff is required. The successful individual will demonstrate a strong record of clinical achievements, as well as experience conducting, designing or serving as a principal investigator for clinical trials. [ back ]
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