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    Site Director - Ohio, 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


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