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US-NJ: Livingston-Associate Director Clinical Research

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Job Title:     Associate Director Clinical Research
Job Location:  NJ: Livingston
Pay Rate:      Open
Job Length:    full time
Start Date:    2007-04-22

Company Name:  The Cambridge Group Ltd.
Contact:       Stephanie Oscar
Phone:         E-mail or fax only
Fax:           203-226-3856

Description:   Associate Director Clinical Research

The AD Clinical Research Oncology will provide scientific, medical and operational expertise to lead multidisciplinary teams and to de-sign and implement high quality programs on time and within budget.  Responsibilities include: guides development of advanced ideas into final product; works toward long- range goals and objectives with consultative direction; may manage and coach 0-5 direct reports including Clinical Research Scientists (CRS) and Senior Clinical Research Scientists (SCRS); contribute and/or lead multidisciplinary task forces to support continuous improvement; responsible for justification of program financial resources in liaison with medical director, clinical operations or Program Operations Manager (POM); may serve as Clinical Trial Leader, globally, a CTL for non-registration local trials, or as a Local Trial Leader in the US; within the global organization, provide clinical research and operational expertise in the creation and execution of overall strategy and objectives of the global clinical development plan. Qualifications include: a Four-year university degree (BA/BS) in Life Sciences/Nursing or equivalent (MS or PhD preferred); at least 5 years experience in clinical development, with at least 3 years of management experience; the ability to analyze and interpret efficacy and safety data; knowledge of advanced clinical trial design; basic statistics and pharmacokinetics; solid medical/scientific writing skills; ability to effectively communicate across the business organization; proficient in all aspects of the clinical development process; medical, scientific and state of the art clinical research knowledge of Oncology; knowledge of GCP/ICH and world wide regulatory requirements relating to assigned area; proven ability to lead cross-functional teams; and the ability to manage and develop people.

Please refer to Job code TP4364 when responding to this ad.

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