Overview:
Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
Responsibilities:
* Conduct Internal and External Laboratory related Audits according to Current Applicable Regulations;
* Track Company-wide Regulatory Training, CAPA Investigations and Metrics Analysis;
* Ensure Compliance to Standard Operating Procedures, Regulations and Standards;
* Assist in the creation and maintenance of Controlled Documents; and
* Interact with Internal and External Clients.
Qualifications:
* Bachelor's degree in the science or a related field;
* Experience in Quality Assurance or Laboratory a plus;
* Excellent Written and Verbal Communications skills;
* Attention to Detail and Well Organized;
* Ability to work well in a Team Environment and Independently.
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