Cincinnati, Ohio30+ days ago
Responsibilities : Develop and validate LC-MS/MS, GC-MS, ICP-MS, HPLC methods for small molecule drugs or drug metabolites and biomarkers; Draft study protocols/plans, acquisition methods, and study reports; Supervise all phases of bioassays to support pre-clinical and clinical pharmacokinetics, PD Biomarkers; Supervise technicians for performing method development, validation, and sample analysis; Communicate with internal and external resources for sample receiving, quality control, quality assurance, sponsor correspondence etc. Qualifications : PhD in Chemistry, Biochemistry, Pharmaceutical Sciences or related field; Previous experience with small molecule drug and drug metabolites analysis; Strong project management, compliance, communication, and people skills; Experience with various extraction procedures, such as LLE, SPE, SLE+, immune-capture hybrid extraction, etc.