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Job Title: Sr Director, Clinical Pharmacology
Job Location: MA: Boston
Pay Rate: Open
Job Length: full time
Start Date: 2008-01-24
Company Name: The Cambridge Group Ltd.
Contact: Stephanie Oscar
Phone: E-mail or fax only
Fax: 203-226-3856
Description: The Senior Director will be a seasoned, experienced and effective group manager of the scientific functions and practical governance of a large department. Responsibilities include the maintenance of structural organization within the department, recruitment and retention of staff, as well as the scientific and managerial coordination of its staff to support development teams. Mentor on scientific issues, motivate staff and resolve conflicts. Guide individual goal setting, manage personnel performance, construct draft-budgets, manage approved budgets, oversee hiring activities and approve all work-related travel for the department. Coordinate corporate planning for the publication and patenting activities, optimize department information flow, and supervise the staff, with all incumbent supervisory responsibilities. Provide advanced interpretation of complex clinical pharmacology data, including PK/PD modeling and clinical trial simulations and incorporate any analyses into reports required for regulatory submissions. Coordinate modes of scientific inquiry that graft together the activities of scientists from diverse functional backgrounds to overcome project obstacles and/or advance a scientific field. Develop proposals for specific new science projects and/or business initiatives, coordinate publication and patent submissions (often as corresponding author or primary inventor), develop regulatory strategy for Clinical Pharmacology and interact with regulatory agencies. Superior skills in recruiting quality staff and refining activities to improve productivity across disciplines are also needed. Requirements: outstanding record in multiple development projects; possess a highly evolved understanding of key scientific fields that impinge on primary area(s) of responsibility; experience in interaction with regulatory agencies, including NDA filings; must effectively interact with Sr. Management and integrate activities across the entire organization. A PhD or MD, strongly preferred, with 12 years of productive, relevant experience in Clinical Pharmacology or Experimental Medicine is required.
Please refer to Job code LF4255 when responding to this ad.
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