Proficient in conducting in-vitro ADME experiments (metabolic stability. CYP inhibition, MBI/TDI, PPB, blood/plasma stability etc.) and interpretation of results.
Review in-vitro ADME data and coordinate with key project team members for assigned projects.
Qualification & Experience
Desired profile: M. Pharm (Pharmacology/Pharmaceutical Analysis) / M.Sc. (Biochemistry/Pharmaceutical Chemistry/Analytical Chemistry) with 4-8 years' experience.
Experience of handling various makes of LC-MS/MS systems to support bioanalysis of in vitro ADME sample. • Experience of writing and reviewing SOP's, study protocols and reports forregulatory submission.
Good understanding of drug metabolism and pharmacokinetics. Experience of handling software like MS office, Graph Pad Prism, etc.