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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