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  • New Job Announcement - Please Post


    Announcing a new Research position
    Our client is located in the Philadelphia area and a global leader in the
    orthopedic industry.
    This position has primary responsibility for ensuring the adequacy of
    pre-clinical testing protocols, including non-human in vivo studies. This position
    is also responsible for representing the company on national and
    international standards setting committees and will act as one of the liaisons to the
    academic research communities.
    · Develop and implement standardized processes for the timely
    construction of pre-clinical safety and performance studies as required by ongoing
    product development and regulatory projects.
    · Represent the company and participate on national and
    international standards establishment committees (i.e., ASTM, ANSI, ICH, etc.)
    · Assist academic and clinical researchers in the construction and
    conduct of scientifically meaningful study protocols
    · Provide guidance and direction in the development of internal
    biomechanical test methodologies
    · Serve as company liaison to FDA on issues concerning scientific
    research and testing
    · Participate, as needed, in the identification, review, and
    research of emerging or innovative technologies
    · Know and follow all laws and policies that apply to one's job, and
    maintain the highest levels of professionalism, ethics and compliance at all
    times.
    · PROFESSIONAL EXPERIENCE REQUIREMENTS:
    · PhD with a minimum 5 years of prior experience in the research and
    development of orthopedic or osteo-biologic technologies
    · Demonstrated understanding of the potential effects of alternative
    or innovative biomaterials, biologics and/or therapeutics
    · Demonstrated ability to build professional relationships within
    the academic and clinical research communities
    · Proven track record of the authoring and/or critical review of
    scientific publications
    · Strong knowledge of FDA Medical Device Regulations and Guidances
    PLEASE SEND A RESUME IN A WORD DOCUMENT TO:
    Nancy Rowe
    MRP
    _Nrowe1@aol.com_ (mailto:Nrowe1@aol.com)
    (724) 335-4544 Phone

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