Master’s degree in biology, chemistry, biochemistry, pharmaceutical science, pharmacology, or other related scientific discipline or Bachelor’s degree in these same disciplines and a minimum of 2 years of experience and progressively responsible experience in regulated bioanalysis of clinical / preclinical samples (plasma, urine, cells etc.). Demonstrated experience applying analytical techniques to the regulated bioanalysis of clinical / preclinical samples (plasma, urine, cells etc.) using LC-MS/MS, quantitative PCR (qPCR), ELISA, Mesoscale Discovery (MSD) and flow cytometry techniques.