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    Site Director - Houston, United States - Mantell Associates

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    Description
    Mantell Associates is partnered with a leading CRO in their search for a Site Director to join their team.


    Site Director - Responsibilities:
    Oversee day to day operations and GMP manufacturing activities
    Build out a large team of top manufacturing professionals
    Work directly with the COO and board in overseeing successful delivery of projects
    Continually lead the expansion of the facility and the wider business


    Site Head - Requirements:
    B.A. or B.S. required, advanced degree preferred
    Minimum of 3 years' experience in managing clinical trials
    Understand regulatory requirements, as well as Good Clinical Practices (GCP), HIPAA and International Conference on Harmonization (ICH) guidelines
    Able to communicate with providers, co-workers, sponsors, and others in a collaborative and courteous manner
    Knowledgeable in medical terminology to communicate with physician offices, pharmacists and laboratory staff
    Able to manage a staff of clinical professionals and create a productive, satisfying work environment
    Demonstrate the initiative to act independently, initiating activity as required and making appropriate decisions within the constraints of study protocols, regulatory requirements, and company policy
    Excellent communication skills (interpersonal, written, verbal)
    Ability to perform overnight business travel
    Good organizational and interpersonal skills
    Attention to detail
    Excellent Computer Skills to include Word, Excel, PowerPoint, as well as proprietary applications unique to the clinical research industry (such as Study Manager)

    Mantell Associates is a specialist Pharmaceutical and Life Sciences headhunting firm. For more information on this role, please contact us at

    #J-18808-Ljbffr

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