Extensive experience (7-9 yrs with masters, 2-5 years with Ph.d.) in a wide variety of in vitro ADME assays (PPB, Microsomal stability, hepatocyte stability etc), and deep fundamental understanding of mechanistic ADME, including a solid track record in applying new science and technologies to enhance in vitro ADME assays.
Should able to perform the assay individually and guide the team to perform these assays as per client requirement.
Able to understand the bioanalytical data and do assay troubleshooting of various technical aspects as and when required.
Strong communication skills and should have experiences in supporting novel modalities and managing in vitro ADME assays.
Prior experience conducting ADME assays and understanding of the concept of metabolism is preferred.
Analyze data and maintain detailed, accurate and comprehensible study documentations.
Strong communication skills and should have experiences in supporting novel modalities and managing in vitro ADME assays.
Ability to clearly communicate and work collaboratively with others.
Able to independently interpret findings and make presentations at internal and external meetings.
The individual is expected to be proactive, organized, and passionate about ADME/drug disposition.
