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:
* Monitor laboratory operations in order to verify that accurate, precise, and medically-reliable data are being generated;
* Interact with corporate leadership, administration, government agencies, accrediting agencies, and potential sponsors/clients to gain information and knowledge required to make appropriate business and/or operational recommendations and decisions;
* Ability to troubleshoot technical issues;
* Ability to meet aggressive timelines;
* Oversee the design, validation and maintenance of analytical methods in clinical trial environments;
* Oversee the analysis of laboratory testing; and
* Oversee technical areas (i.e., Clinical Chemistry/Hematology/Coagulation/ELISA).
Qualifications:
* PhD in Laboratory Medicine, Immunology, Clinical Chemistry, Clinical Pathology, Biomedical Sciences or other similar area;
* Experience in automation of data analysis, statistical analysis and/or computer databse programming is considered a plus;
* Excellent project management and communication skills;
* Proficiency in English is required;
* Experience in a Central Laboratory setting or with clinical research preferred;
* Candidates with experience in genomics are welcome to apply as well.
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