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:
* Perform low, moderate, and high-complexity clinical testing following applicable SOPs.
* Perform necessary quality control procedures, properly evaluate control data, and implement and document corrective action as needed.
* Perform routine instrument maintenance and troubleshooting;
* Gain knowledge of dederal regulations regarding clinical trials;
* Gain knowledge of pre-analytical variables affecting clinical laboratory testing;
* Gain knowledge of disease states and correlation with clinical laboratory data;
* Perform testing, documentation, and routine lab system operations; and
* Ensure validity of laboratory data reported.
Qualifications:
* A minimum of a bachelor's degree with relevant experience in molecular biology, genetics, genomics or equivalent.
* 2-5 years of Laboratory/Medical Technologist experience
* MT (ASCP), MLS (ASCP), or CLS (NCA) certification (preferred, if applicable);
* Familiarity with basic molecular biology techniques (PCR, RT-PCR, DNA and RNA extraction);
* Laboratory experience of DNA/RNA sequencing is a plus
* Excellent written and verbal communication skills
* Able to work in a team environment with effective interpersonal skills and able to work independently.
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