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.
- Perform routine instrument maintenance and troubleshooting;
- Expected to develop knowledge of local and international regulations regarding clinical trials;
- Expected to develop knowledge of pre-analytical variables affecting clinical laboratory testing;
- Expected to develop knowledge of disease processes and correlation with clinical laboratory data;
- Perform laboratory investigations;
- Perform clinical specimen testing, documentation, and routine lab system operations; and
- Ensure validity of laboratory data reported.
- Bachelor of Science degree with at least 2 years of hands-on experience in Biochemistry, Haematology, and/or Immunology;
- Basic knowledge of drug therapy techniques and medical terminology;
- Excellent written and verbal communication skills;
- Able to work in a team environment with effective interpersonal skills and able to work independently; and
- Able to work on rotational public holidays and weekends.
